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FDA 510(k)

RED CAP, M-502

K-Number: K791851 · 1979-10-01

ApplicantMem Medical, Inc.
Decision Date1979-10-01
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RED CAP, M-502 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 K791851. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RED CAP, M-502?

RED CAP, M-502 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 K791851.

When did RED CAP, M-502 receive FDA 510(k) clearance?

RED CAP, M-502 received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791851.

Who is the listed applicant for RED CAP, M-502?

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 RED CAP, M-502?

The FDA product code for RED CAP, M-502 is BYX.

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

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Related Devices (Code: BYX)

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.

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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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