FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

Capnostream 35 Portable Respiratory Monitor

K Number: K150272 · Decision Jul 17, 2015
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
19
Review Days
163

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Basic Information

Device Name
Capnostream 35 Portable Respiratory Monitor
K Number
K150272
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oridion Medical 1987 , Ltd.
Date Received
February 4, 2015
Decision Date
July 17, 2015
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

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

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Other Clearances by Oridion Medical 1987 , Ltd.

K Number Device Name
K200594 Capnostream 35 Portable Respiratory Monitor
K181624 Microstream Advance Neonatal-Infant Nasal Filter Line with O2 Tubing, Microstream Advance Pediatric Oral-Nasal Filter Line with O2 Tubing, Microstream Advance Adult Oral-Nasal Filter Line with O2 Tubing, Microstream Luer Adult Oral-Nasal Sampling Line
K181467 Microstream Luer Adult-Pediatric Intubated Sampling Line, Microstream Advance Adult-Pediatric Intubated Filter Line
K123690 CAPNOSTREAM20P WITH HIFI C02 MONITORING
K121927 MICROSTREAM FILTERLINE ICU
K112368 CAPNOSTREAM20P WITH AI/ODI
K093388 SMART CAPNOLINE GUARDIAN
K042665 SMART BITEBLOC
K024300 MICROCAP PLUS/NPB-75
K013845 MODIFICATION TO: MAC-LINE O2/CO2 ORAL NASAL CANNULA SAMPLE LINE
Search all 19 clearances from Oridion Medical 1987 , Ltd. →