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

PI-PNEUMO-INTESTINAL INSTRUMENT SET

K Number: K823776 · Decision Jan 14, 1983
Classifications
1
FEI Numbers
76
Registration Numbers
76
Same Product Code
41
Applicant Total
6
Review Days
30

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
PI-PNEUMO-INTESTINAL INSTRUMENT SET
K Number
K823776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Surgeons Choice, Inc.
Date Received
December 15, 1982
Decision Date
January 14, 1983
Product Code
GAG
Advisory Committee
General Hospital
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
GAG Stapler, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Surgeons Choice, Inc.

K Number Device Name
K851121 PI-PHEUMO INTESTINAL INSTRUMENT SET
K851122 PI-PNEUMO INTESTINAL STAPLING CARTRIDGE
K843399 SURGEONS CHOICE PI VASCULAR STAPLING
K830768 DISPOSABLE SKIN STAPLER
K813170 ILA(INVERTED LINEAR ANASTOMOSIS) STAPLER