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

NORMCAP CD-102, CARBON DIOXIDE ANALYZER

K Number: K801083 · Decision May 28, 1980
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
2
Review Days
21

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Basic Information

Device Name
NORMCAP CD-102, CARBON DIOXIDE ANALYZER
K Number
K801083
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Instrumentarium-Datex
Date Received
May 7, 1980
Decision Date
May 28, 1980
Product Code
CCL
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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Similar 510(k) Clearances

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

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Other Clearances by Instrumentarium-Datex

K Number Device Name
K802762 NORMOCAP CR-102, RECORDER UNIT