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

MODEL CD-3A-INCLUDING P-61B SENSOR

K Number: K833060 · Decision Nov 3, 1983
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
1
Review Days
56

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MODEL CD-3A-INCLUDING P-61B SENSOR
K Number
K833060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Applied Electrochemistry, Inc.
Date Received
September 8, 1983
Decision Date
November 3, 1983
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.

View all