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

DESERET ARTERIAL BLOOD SAMPLING KIT

K Number: K822248 · Decision Oct 21, 1982
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
57
Applicant Total
50
Review Days
84

Basic Information

Device Name
DESERET ARTERIAL BLOOD SAMPLING KIT
K Number
K822248
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1100
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
WARNER-LAMBERT CO.
Date Received
July 29, 1982
Decision Date
October 21, 1982
Product Code
CBT
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBT Arterial Blood Sampling Kit

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