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Product Description
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Recall Class
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FDA Recall Posting Date
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Recalling Firm
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Z-0526-05 - Dental Explorer #2 D/E, Mfr. Part Code/Product Code 101-0913, distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B057701. Pr...
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2
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02/04/2005
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FEI # 1416605 Hu-Friedy Mfg Co, Inc.
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Z-0529-05 - Dental Explorer Single End #7, Mfr. Part Code/Product Code 100-7409. Distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B0...
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2
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02/04/2005
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FEI # 1416605 Hu-Friedy Mfg Co, Inc.
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Z-0528-05 - Dental Explorer D/E #5, Mfr. Part Code/Product Code 100-8008, distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B057701. T...
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2
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02/04/2005
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FEI # 1416605 Hu-Friedy Mfg Co, Inc.
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Z-0527-05 - Dental Explorer #23 S/E, Mfr. Part Code/Product Code 100-3620, distributed under the Henry Schein label. Classification Name: 21CFR 872.4565; 510(k) exempt, Class I device, Device Listing # B057701. ...
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2
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02/04/2005
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FEI # 1416605 Hu-Friedy Mfg Co, Inc.
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