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

SURVIVAL KIT, INDIVIDUAL

K Number: K871437 · Decision Jul 9, 1987
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
23
Review Days
87

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
SURVIVAL KIT, INDIVIDUAL
K Number
K871437
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Fraass Survival Systems, Inc.
Date Received
April 13, 1987
Decision Date
July 9, 1987
Product Code
LRO
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
LRO General Surgery Tray

Similar 510(k) Clearances

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

View all

Other Clearances by Fraass Survival Systems, Inc.

K Number Device Name
K912022 FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES
K871434 MEDICAL PACKET, INDIVIDUAL SURVIVAL KIT, AIRMAN'S
K871458 SURVIVAL KIT, INDIVIDUAL, TROP, TACTICAL AIR CREW
K871917 FRASTEC DRY GAUZE BANDAGE
K871916 FRASTEC DRY BURN DRESSING
K871376 FIRST AID KIT, VARIOUS SIZES
K871501 KIT, FIRST AID, GENERAL PURPOSE, RIGID CASE
K871457 FIRST AID KIT, EYE DRESSING
K871438 BANDAGE, MUSLIN, COMPRESSED, CAMOUFLAGED 37X37X52
K870240 COMPRESS AND SKULLCAP, HEAD DRESSING
Search all 23 clearances from Fraass Survival Systems, Inc. →