FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BARRIER BURN SHEET

K Number: K821835 · Decision Jul 2, 1982
Classifications
1
FEI Numbers
573
Registration Numbers
573
Same Product Code
64
Applicant Total
3
Review Days
10

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Basic Information

Device Name
BARRIER BURN SHEET
K Number
K821835
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6060
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Uhi Corp.
Date Received
June 22, 1982
Decision Date
July 2, 1982
Product Code
KME
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
KME Bedding, Disposable, Medical

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Other Clearances by Uhi Corp.

K Number Device Name
K843389 CLINITRON AIR FLUIDIZED SUPPORT J-101UD
K813584 CLINITRON AIR FLUIDIZED SUPPORT SYSTEM