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

NEONATAL METASCOPE

K Number: K903959 · Decision Nov 23, 1990
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
11
Review Days
87

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Basic Information

Device Name
NEONATAL METASCOPE
K Number
K903959
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1850
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Cybermedic, Inc.
Date Received
August 28, 1990
Decision Date
November 23, 1990
Product Code
BZK
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
BZK Spirometer, Monitoring (W/Wo Alarm)

Similar 510(k) Clearances

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Other Clearances by Cybermedic, Inc.

K Number Device Name
K941813 VENSHIELD
K914205 PFF-1
K884910 MODEL 1010, CY-MET
K861418 SPINNAKER
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. →