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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K827086
Device Name LATERAL ANGULATING FLUORO SUSPENSION
Applicant
General Electric Co.
1 River Rd.
Schenectady,  NY  12345
Correspondent
General Electric Co.
1 River Rd.
Schenectady,  NY  12345
Date Received01/22/1982
Decision Date 02/24/1982
Decision Substantially Equivalent (SESE)
510k Review Panel Radiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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