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FDA 510(k)

MANIFOLD CLAMPS

K-Number: K852118 · 1985-06-06

ApplicantOmser Sv., Inc.
Decision Date1985-06-06
Product CodeDTL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MANIFOLD CLAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Omser Sv., Inc.. It received FDA 510(k) clearance on 1985-06-06 under 510(k) number K852118. 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 MANIFOLD CLAMPS?

MANIFOLD CLAMPS is a medical device that received FDA 510(k) clearance on 1985-06-06. The listed applicant is Omser Sv., Inc.. The 510(k) number is K852118.

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

MANIFOLD CLAMPS received FDA 510(k) clearance on 1985-06-06, under 510(k) number K852118.

Who is the listed applicant for MANIFOLD CLAMPS?

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

What is the FDA product code for MANIFOLD CLAMPS?

The FDA product code for MANIFOLD CLAMPS 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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