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

SPINNAKER

K Number: K861418 · Decision May 9, 1986
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
89
Applicant Total
11
Review Days
24

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Basic Information

Device Name
SPINNAKER
K Number
K861418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1880
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Cybermedic, Inc.
Date Received
April 15, 1986
Decision Date
May 9, 1986
Product Code
BZC
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
BZC Calculator, Pulmonary Function Data

Similar 510(k) Clearances

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

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Other Clearances by Cybermedic, Inc.

K Number Device Name
K941813 VENSHIELD
K914205 PFF-1
K903959 NEONATAL METASCOPE
K884910 MODEL 1010, CY-MET
K851197 CYBERMEDIC CM-810 BODY PLETHYSMOGRAPH
K842782 PHYSIOLOGICAL ANALYZER CM-710
K842760 LUNG ANALYZER CM-310
K831586 CM-VII PHYSIOLOGIC ANALYZER
K800547 MEDISTOR III LUNG ANALYZER
K790579 MEDISTOR II
Search all 11 clearances from Cybermedic, Inc. →