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

BURDICK PRO2 OXIMETER

K Number: K941351 · Decision Oct 13, 1994
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
38
Review Days
205

Basic Information

Device Name
BURDICK PRO2 OXIMETER
K Number
K941351
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BURDICK CORP.
Date Received
March 22, 1994
Decision Date
October 13, 1994
Product Code
DQA
Advisory Committee
Cardiovascular
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
DQA Oximeter

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