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

SCREENING COMPUTEO SC-20

K Number: K771371 · Decision Aug 4, 1977
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
25
Applicant Total
32
Review Days
10

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Basic Information

Device Name
SCREENING COMPUTEO SC-20
K Number
K771371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1900
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Cavitron Corp.
Date Received
July 25, 1977
Decision Date
August 4, 1977
Product Code
BZM
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
BZM Calculator, Pulmonary Function Interpretor (Diagnostic)

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Other Clearances by Cavitron Corp.

K Number Device Name
K811582 THE PLACER
K810207 MINOR SURGERY LIGHT
K802928 SPIROMETRIC COMPUTER #SC-10
K801623 CAVITRON ULTRASONIC SURG. ASPIR. CUSA
K801877 SLIT LAMP ATTACHMENT
K800869 MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA
K800722 AUTO-FIELD D AUTOMATED VISUAL DETECTOR
K791585 MODEL G-61 ULTRASONIC DENTAL UNIT
K791277 MODEL 6500 EXTRACTION IRRIGATION SYS
K782054 LASER, CO2 SURGICAL
Search all 32 clearances from Cavitron Corp. →