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

STERILE SURGICAL DRAPES

K Number: K821666 · Decision Jun 21, 1982
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
2
Applicant Total
6
Review Days
14

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Basic Information

Device Name
STERILE SURGICAL DRAPES
K Number
K821666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Phoenix Glove Co.
Date Received
June 7, 1982
Decision Date
June 21, 1982
Product Code
FJZ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FJZ Declotting Tray, Kit (Including Contents)

Similar 510(k) Clearances

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

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Other Clearances by Phoenix Glove Co.

K Number Device Name
K830660 STERILE SURGICAL DRAPES
K821044 PATIENT PREP KITS/TRAYS-STERILE
K821043 STERILE PATIENT EXAM. GLOVES
K801846 ELECTROCARDIOGRAPH ELECTRODE
K781820 GLOVES, VINYL EXAMINATION