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

CONTAIN-OR

K Number: K934215 · Decision Feb 9, 1994
Classifications
1
FEI Numbers
200
Registration Numbers
200
Same Product Code
449
Applicant Total
56
Review Days
163

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Basic Information

Device Name
CONTAIN-OR
K Number
K934215
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
Dlp, Inc.
Date Received
August 30, 1993
Decision Date
February 9, 1994
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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K Number Device Name
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K953945 RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET
K950754 MACRO SUCTION TUBE MODEL NO 10061
K915268 CATHETER TWO STAGE VENOUS RETURN
K913077 LANCASTER COOLING JACKET, CAT. CODE #13500/13501
K914608 BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120
K913098 APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501
K912229 IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003
K904172 ACCUPLACE (TM)
Search all 56 clearances from Dlp, Inc. →