FDA 510(k) FDA not classified Substantially Equivalent 🇺🇸 United States

FIRST AID/TRUMA KIT

K Number: K941311 · Decision Jun 14, 1994
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
14
Applicant Total
17
Review Days
88

Basic Information

Device Name
FIRST AID/TRUMA KIT
K Number
K941311
Device Class
FDA not classified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CERTIFIED SAFETY MFG., INC.
Date Received
March 18, 1994
Decision Date
June 14, 1994
Product Code
LRR
Advisory Committee
Unknown
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
LRR First Aid Kit With Drug

Similar 510(k) Clearances

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Other Clearances by CERTIFIED SAFETY MFG., INC.

K Number Device Name
K960587 CPROTECTOR 2000
K960615 GAUZE COMPRESS
K960624 CERTI COOL INSTANT COLD COMPRESS
K953102 BLOODBORNE PATHOGEN KIT
K946338 CERTIBURN BURN/TRAUMA FACE DRESSING, TOWEL DRESSING
K945002 1X6YD, 2X6YD, 4X6YD ROLL BANDAGE
K945004 2, 3 & 4 BANDADGE COMPRESS
K940249 CERTIBURN BURN/TRAUMA FACE DRESSING /TOWEL DRESSING
K940358 X-LARGE MULTI-FUNCTION TRAUMA DRESSING
K940333 EYE PAD
Search all 17 clearances from CERTIFIED SAFETY MFG., INC. →