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

STERILE PLASTIC DRAPE

K Number: K913408 · Decision Mar 12, 1992
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
12
Review Days
226

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Basic Information

Device Name
STERILE PLASTIC DRAPE
K Number
K913408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acacia Laboratories, Inc.
Date Received
July 30, 1991
Decision Date
March 12, 1992
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

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Other Clearances by Acacia Laboratories, Inc.

K Number Device Name
K952419 STERIGAUZE GEL DRESSING
K952420 STERIGAUZE WET DRESSING
K951861 STERICARE WOUND CARE GEL
K952414 PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETER
K951914 HYDRACARE ABSORBENT WOUND DRESSING
K950344 HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETER
K901761 STERILE SUCTION TUBING SET
K892856 NEWMARK(TM) CORONARY ARTERY BYPASS GRAFT MARKERS
K892804 NEWCHILL(TM) CARDIAC INSULATOR
K884055 SURGI-TAG(TM) STERILE LABEL SETS
Search all 12 clearances from Acacia Laboratories, Inc. →