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FDA 510(k)

MONOMER VAPOR CONTAINMENT SYSTEM

K-Number: K760906 · 1976-11-11

Decision Date1976-11-11
Product CodeJDY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MONOMER VAPOR CONTAINMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1976-11-11 under 510(k) number K760906. The device is classified under product code JDY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONOMER VAPOR CONTAINMENT SYSTEM?

MONOMER VAPOR CONTAINMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1976-11-11. The listed applicant is Howmedica Corp.. The 510(k) number is K760906.

When did MONOMER VAPOR CONTAINMENT SYSTEM receive FDA 510(k) clearance?

MONOMER VAPOR CONTAINMENT SYSTEM received FDA 510(k) clearance on 1976-11-11, under 510(k) number K760906.

Who is the listed applicant for MONOMER VAPOR CONTAINMENT SYSTEM?

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 MONOMER VAPOR CONTAINMENT SYSTEM?

The FDA product code for MONOMER VAPOR CONTAINMENT SYSTEM is JDY.

Related Clinical Trials

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.

Other records listing Howmedica 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.

View all 373 devices →

Related Devices (Code: JDY)

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.

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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