FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

K Number: K930286 · Decision Jun 22, 1993
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
57
Applicant Total
23
Review Days
152

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Basic Information

Device Name
DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS
K Number
K930286
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.1100
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Summary
Applicant
Concord/Portex
Date Received
January 21, 1993
Decision Date
June 22, 1993
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

Similar 510(k) Clearances

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Other Clearances by Concord/Portex

K Number Device Name
K923559 STERI-CATH MDI
K930218 SUBCUTANEOUS TUNNELING NEEDLE AND HANDLES
K924541 EPIDURAL MINIPACK
K923127 NEEDLE-PRO CARTRIDGE
K923910 HEAT MOISTURE CONDENSER
K922749 LOW PROFILE TRACHEOSTOMY TUBE
K922445 VACU-PRO
K915452 ANESTHESIA BREATHING CIRCUIT
K911809 NEW-VENT
K912124 TRACHEOSTOMY TUBE AND CUFF
Search all 23 clearances from Concord/Portex →