FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

GRICE LAPAROSCOPIC SUTURING NEEDLE

K Number: K921922 · Decision Jul 8, 1992
Classifications
1
FEI Numbers
548
Registration Numbers
548
Same Product Code
1422
Applicant Total
16
Review Days
76

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Basic Information

Device Name
GRICE LAPAROSCOPIC SUTURING NEEDLE
K Number
K921922
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ideal Medical, Inc.
Date Received
April 23, 1992
Decision Date
July 8, 1992
Product Code
GCJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GCJ Laparoscope, General & Plastic Surgery

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