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FDA 510(k)

TEE- TWO-WAY VALVES M-500

K-Number: K791853 · 1979-10-01

ApplicantMem Medical, Inc.
Decision Date1979-10-01
Product Code
DecisionSubstantially Equivalent

Device Summary

TEE- TWO-WAY VALVES M-500 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 1979-10-01 under 510(k) number K791853. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEE- TWO-WAY VALVES M-500?

TEE- TWO-WAY VALVES M-500 is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Mem Medical, Inc.. The 510(k) number is K791853.

When did TEE- TWO-WAY VALVES M-500 receive FDA 510(k) clearance?

TEE- TWO-WAY VALVES M-500 received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791853.

Who is the listed applicant for TEE- TWO-WAY VALVES M-500?

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

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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.

K791907RETARD VALVE 3-STACK #M-515K791909IMV BUSHING #M-513K791913IMV MANIFOLD #M-506K791904IMV W/BAG & HOSES #M-509K791908RETARD VALVE 3-STACK #M-514K791912IMV FOR MONITORING #M-510

View all 27 devices →

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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