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FDA 510(k)

SCREENING COMPUTEO SC-20

K-Number: K771371 · 1977-08-04

ApplicantCavitron Corp.
Decision Date1977-08-04
Product CodeBZM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SCREENING COMPUTEO SC-20 is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-08-04 under 510(k) number K771371. The device is classified under product code BZM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCREENING COMPUTEO SC-20?

SCREENING COMPUTEO SC-20 is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Cavitron Corp.. The 510(k) number is K771371.

When did SCREENING COMPUTEO SC-20 receive FDA 510(k) clearance?

SCREENING COMPUTEO SC-20 received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771371.

Who is the listed applicant for SCREENING COMPUTEO SC-20?

The FDA 510(k) record lists Cavitron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCREENING COMPUTEO SC-20?

The FDA product code for SCREENING COMPUTEO SC-20 is BZM.

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Other records listing Cavitron Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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Related Devices (Code: BZM)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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