FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

VARIOUS STERILE CUSTOM DRESSING TRAYS & KITS

K Number: K912351 · Decision Jun 17, 1993
Classifications
1
FEI Numbers
151
Registration Numbers
151
Same Product Code
1953
Applicant Total
5
Review Days
751

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Basic Information

Device Name
VARIOUS STERILE CUSTOM DRESSING TRAYS & KITS
K Number
K912351
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6250
Medical Specialty
General Hospital
Decision
Unknown
Statement or Summary
Statement
Applicant
Surgipro, Inc.
Date Received
May 28, 1991
Decision Date
June 17, 1993
Product Code
LYY
Advisory Committee
General Hospital
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
LYY Latex Patient Examination Glove

Similar 510(k) Clearances

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

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Other Clearances by Surgipro, Inc.

K Number Device Name
K934031 STERILE CENTRAL LINE DRESSING TRAY
K934028 STERILE DRESSING CHANGE TRAY
K934029 STERILE LACERATION & DEBRIDEMENT TRAYS
K934030 STERILE TRACHEOSTOMY TRAY