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

CAPNOCHECK II, MODEL 8400

K Number: K991086 · Decision Jun 9, 1999
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
304
Applicant Total
20
Review Days
70

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Basic Information

Device Name
CAPNOCHECK II, MODEL 8400
K Number
K991086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1400
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bci Intl., Inc.
Date Received
March 31, 1999
Decision Date
June 9, 1999
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

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Other Clearances by Bci Intl., Inc.

K Number Device Name
K991410 3402 HANDHELD PULSE OXIMETER
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K983796 6004 NIBP MONITOR WITH TEMPERATURE
K982279 VITAL SIGNS MONITOR; ADVISOR MODEL # BCI 9200
K981939 AUTOCORR PLUS; 3404 OXIMETER/ECG MONITOR
K980714 BCI 3401 HANDHELD PULSE OXIMETER
K974697 REUSABLE FINGER SENSOR 3444
K970801 BCI MODEL 6004 NIBP MONITOR (6004)
K970209 CAPNOCHECK PLUS
K963496 OXI TEMP
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