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FDA 510(k)

MOLICARE

K-Number: K843405 · 1984-10-19

Decision Date1984-10-19
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MOLICARE is the device name listed in this FDA 510(k) record. The listed applicant is Paul Hartmann Corp.. It received FDA 510(k) clearance on 1984-10-19 under 510(k) number K843405. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOLICARE?

MOLICARE is a medical device that received FDA 510(k) clearance on 1984-10-19. The listed applicant is Paul Hartmann Corp.. The 510(k) number is K843405.

When did MOLICARE receive FDA 510(k) clearance?

MOLICARE received FDA 510(k) clearance on 1984-10-19, under 510(k) number K843405.

Who is the listed applicant for MOLICARE?

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

What is the FDA product code for MOLICARE?

The FDA product code for MOLICARE is EYQ.

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 Paul Hartmann 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.

Related Devices (Code: EYQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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