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

ARC

K Number: K934669 · Decision Apr 26, 1994
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
8
Review Days
209

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Basic Information

Device Name
ARC
K Number
K934669
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5160
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medelec , Ltd.
Date Received
September 29, 1993
Decision Date
April 26, 1994
Product Code
BSZ
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
BSZ Gas-Machine, Anesthesia

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Other Clearances by Medelec , Ltd.

K Number Device Name
K965065 TECA. MILLENNIUM
K964280 DG NERVUS
K954157 DG PORTABLE SYSTEM
K953799 DG EXAMINER PLUS
K953732 TECA PREMIERE
K934670 DG 3P SYSTEM
K923303 SAPPHIRE PREMIERE