FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LSVP INTERNATIONAL BIOPSY FORCEPS

K Number: K944770 · Decision Oct 13, 1994
Classifications
1
FEI Numbers
188
Registration Numbers
188
Same Product Code
38
Applicant Total
4
Review Days
16

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Basic Information

Device Name
LSVP INTERNATIONAL BIOPSY FORCEPS
K Number
K944770
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.1075
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lsvp Intl., Inc.
Date Received
September 27, 1994
Decision Date
October 13, 1994
Product Code
FCL
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FCL Forceps, Biopsy, Non-Electric

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FCL), ordered by most recent decision date.

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Other Clearances by Lsvp Intl., Inc.

K Number Device Name
K982983 LSVP INTERNATIONAL BIOPSY FORCEPS
K971204 LSVP INTERNATIONAL HOT BIOPSY FORCEPS
K945295 LSVP INTERNATIONAL GRASPING FORCEPS