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

TOWEL DRAPE, MODELS 4409, 4410

K Number: K012957 · Decision Mar 6, 2002
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
19
Review Days
183

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
TOWEL DRAPE, MODELS 4409, 4410
K Number
K012957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dynarex Corp.
Date Received
September 4, 2001
Decision Date
March 6, 2002
Product Code
KKX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KKX Drape, Surgical, Antimicrobial

Similar 510(k) Clearances

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

View all

Other Clearances by Dynarex Corp.

K Number Device Name
K052743 DYNAREX CPR SHIELD WITH ONE WAY VALVE AND BARRIER FILTER, MODEL 4921
K052314 DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
K012816 DYNAREX IODOFORM PACKING STRIPS, MODELS 3411, 3412, 3413, 3414
K012917 DYNAREX UMBILICAL CORD LAMP, MODELS 6833 AND 6833-B
K991695 DYNAREX NON-WOVEN SPONGE
K991694 DYNAREX DRAIN SPONGE
K983348 DYNAREX TRACHEOSTOMY SPONGE
K960388 DYNAREX NON-WOVEN SPONGE
K951660 DYNAREX GAUZE SPONGE
K933308 DYNAREX GAUZE SPONGE OR PADS
Search all 19 clearances from Dynarex Corp. →