FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MASS SPECTROMETRY MONITORING LINES AND CONNECTORS

K Number: K900291 · Decision Mar 28, 1990
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
4
Review Days
65

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Basic Information

Device Name
MASS SPECTROMETRY MONITORING LINES AND CONNECTORS
K Number
K900291
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
F.L.W. Plastics, Inc.
Date Received
January 22, 1990
Decision Date
March 28, 1990
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 F.L.W. Plastics, Inc.

K Number Device Name
K895233 BACTERIAL AND VIRAL FILTER
K895357 ANETHESIA BREATHING CIRCUIT
K895169 MANUAL DISPOSABLE PULMONARY RESUSCITATOR