FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

BAWMED RESCUE MASK

K Number: K031431 · Decision Jul 13, 2004
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
102
Applicant Total
2
Review Days
434

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Basic Information

Device Name
BAWMED RESCUE MASK
K Number
K031431
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5870
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bawmed UK
Date Received
May 6, 2003
Decision Date
July 13, 2004
Product Code
CBP
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
CBP Valve, Non-Rebreathing

Similar 510(k) Clearances

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

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Other Clearances by Bawmed UK

K Number Device Name
K031434 BAWMED E-Z BAG RESUSCITATOR