FDA 510(k)

HEMOREST(TM)

K-Number: K864470 · 1987-06-23

Decision Date1987-06-23

Product CodeLRL

DecisionSubstantially Equivalent

Device Summary

HEMOREST(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Health Aid Products. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K864470. The device is classified under product code LRL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOREST(TM)?

HEMOREST(TM) is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Health Aid Products. The 510(k) number is K864470.

When did HEMOREST(TM) receive FDA 510(k) clearance?

HEMOREST(TM) received FDA 510(k) clearance on 1987-06-23, under 510(k) number K864470.

Who is the listed applicant for HEMOREST(TM)?

The FDA 510(k) record lists Health Aid Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEMOREST(TM)?

The FDA product code for HEMOREST(TM) is LRL.

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.

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Related Devices (Code: LRL)

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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.