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

FIRST AID KITS

K Number: K831795 · Decision Sep 1, 1983
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
41
Review Days
90

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
FIRST AID KITS
K Number
K831795
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
I M, Inc.
Date Received
June 3, 1983
Decision Date
September 1, 1983
Product Code
KDD
Advisory Committee
General, Plastic Surgery
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
KDD Kit, Surgical Instrument, Disposable

Similar 510(k) Clearances

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

View all

Other Clearances by I M, Inc.

K Number Device Name
K914600 NEUROLOGICAL SPONGE
K892389 BIOPSY KIT
K881363 SYRINGE PREFILLED WITH WATER
K880753 UMBILICAL CORD CLAMP
K872741 NUTRIPUMP
K871495 BANDAGES CATALOG NUMBER: 101 TO 220
K863785 MAKLER CATHETER
K854155 STERILE SALINE SOLUTION
K853287 HUBOUT
K853288 FEEDING UNITS & TUBES
Search all 41 clearances from I M, Inc. →