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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Ward Use, Portable, Ac-Powered
510(k) Number K920288
Device Name POWERED VACUUM ASPIRATOR 1110-G-062
Applicant
Stirn Industries
1095 Cranbury So. River Rd.
P.O. Box 407
Dayton,  NJ  08810
Applicant Contact ROBERT W HARRINGTON
Correspondent
Stirn Industries
1095 Cranbury So. River Rd.
P.O. Box 407
Dayton,  NJ  08810
Correspondent Contact ROBERT W HARRINGTON
Regulation Number878.4780
Classification Product Code
JCX  
Date Received01/22/1992
Decision Date 06/29/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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