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FDA 510(k)

MONOTUBE TUBE-TO-TUBE CLAMP

K-Number: K954667 · 1996-01-11

ApplicantHowmedica Corp.
Decision Date1996-01-11
Product CodeJEC
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MONOTUBE TUBE-TO-TUBE CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1996-01-11 under 510(k) number K954667. The device is classified under product code JEC. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOTUBE TUBE-TO-TUBE CLAMP?

MONOTUBE TUBE-TO-TUBE CLAMP is a medical device that received FDA 510(k) clearance on 1996-01-11. The listed applicant is Howmedica Corp.. The 510(k) number is K954667.

When did MONOTUBE TUBE-TO-TUBE CLAMP receive FDA 510(k) clearance?

MONOTUBE TUBE-TO-TUBE CLAMP received FDA 510(k) clearance on 1996-01-11, under 510(k) number K954667.

Who is the listed applicant for MONOTUBE TUBE-TO-TUBE CLAMP?

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

What is the FDA product code for MONOTUBE TUBE-TO-TUBE CLAMP?

The FDA product code for MONOTUBE TUBE-TO-TUBE CLAMP is JEC.

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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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