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FDA 510(k)

ANALYZER, 751 KINETIC/ENDPOINT

K-Number: K770306 · 1977-04-05

ApplicantSclavo, Inc.
Decision Date1977-04-05
Product CodeJJQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYZER, 751 KINETIC/ENDPOINT is the device name listed in this FDA 510(k) record. The listed applicant is Sclavo, Inc.. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770306. The device is classified under product code JJQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, 751 KINETIC/ENDPOINT?

ANALYZER, 751 KINETIC/ENDPOINT is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is Sclavo, Inc.. The 510(k) number is K770306.

When did ANALYZER, 751 KINETIC/ENDPOINT receive FDA 510(k) clearance?

ANALYZER, 751 KINETIC/ENDPOINT received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770306.

Who is the listed applicant for ANALYZER, 751 KINETIC/ENDPOINT?

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

What is the FDA product code for ANALYZER, 751 KINETIC/ENDPOINT?

The FDA product code for ANALYZER, 751 KINETIC/ENDPOINT is JJQ.

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Related Devices (Code: JJQ)

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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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