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FDA 510(k)

TRANSPARENT MANIFOLD

K-Number: K772299 · 1977-12-21

ApplicantUni-Research
Decision Date1977-12-21
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TRANSPARENT MANIFOLD is the device name listed in this FDA 510(k) record. The listed applicant is Uni-Research. It received FDA 510(k) clearance on 1977-12-21 under 510(k) number K772299. The device is classified under product code DTL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSPARENT MANIFOLD?

TRANSPARENT MANIFOLD is a medical device that received FDA 510(k) clearance on 1977-12-21. The listed applicant is Uni-Research. The 510(k) number is K772299.

When did TRANSPARENT MANIFOLD receive FDA 510(k) clearance?

TRANSPARENT MANIFOLD received FDA 510(k) clearance on 1977-12-21, under 510(k) number K772299.

Who is the listed applicant for TRANSPARENT MANIFOLD?

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

What is the FDA product code for TRANSPARENT MANIFOLD?

The FDA product code for TRANSPARENT MANIFOLD is DTL.

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Official Source

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

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