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

O.B. BASIN SET

K Number: K843982 · Decision Oct 31, 1984
Classifications
1
FEI Numbers
203
Registration Numbers
203
Same Product Code
316
Applicant Total
27
Review Days
20

Basic Information

Device Name
O.B. BASIN SET
K Number
K843982
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
PRO-LAB, INC.
Date Received
October 11, 1984
Decision Date
October 31, 1984
Product Code
FRG
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
FRG Wrap, Sterilization

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