510(k) K872271

VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS by New England Surgical Instrument Corp. — Product Code GEN

K872271 is an FDA 510(k) premarket notification submitted by New England Surgical Instrument Corp. for the device "VARIOUS SIZES & STYLES OF MONOPOLAR FORCEPS". The FDA issued a decision of Substantially Equivalent on June 26, 1987. The device falls under product code GEN (Forceps, General & Plastic Surgery), a Class I device regulated under 21 CFR 878.4800. New England Surgical Instrument Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 26, 1987
Date Received
June 12, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Forceps, General & Plastic Surgery
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type