FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

ZEFON GAS SAMPLING LINES

K Number: K930957 · Decision Jul 2, 1993
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
4
Review Days
129

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Basic Information

Device Name
ZEFON GAS SAMPLING LINES
K Number
K930957
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Summary
Applicant
Zefon Medical Products
Date Received
February 23, 1993
Decision Date
July 2, 1993
Product Code
CCK
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
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

Similar 510(k) Clearances

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Other Clearances by Zefon Medical Products

K Number Device Name
K940220 REBREATHER BAGS
K934462 ADULT ANESTHESIA BREATHING CIRCUIT KITS
K924889 ZEFON ADULT ANESTHESIA BREATHING CIRCUIT