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FDA 510(k)

RETARD VALVE 3-STACK #M-514

K-Number: K791908 · 1979-10-09

Decision Date1979-10-09
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RETARD VALVE 3-STACK #M-514 is the device name listed in this FDA 510(k) record. The listed applicant is Mem Medical, Inc.. It received FDA 510(k) clearance on 1979-10-09 under 510(k) number K791908. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RETARD VALVE 3-STACK #M-514?

RETARD VALVE 3-STACK #M-514 is a medical device that received FDA 510(k) clearance on 1979-10-09. The listed applicant is Mem Medical, Inc.. The 510(k) number is K791908.

When did RETARD VALVE 3-STACK #M-514 receive FDA 510(k) clearance?

RETARD VALVE 3-STACK #M-514 received FDA 510(k) clearance on 1979-10-09, under 510(k) number K791908.

Who is the listed applicant for RETARD VALVE 3-STACK #M-514?

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

What is the FDA product code for RETARD VALVE 3-STACK #M-514?

The FDA product code for RETARD VALVE 3-STACK #M-514 is CBP.

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 Mem Medical, Inc. 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 27 devices →

Related Devices (Code: CBP)

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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