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FDA 510(k)

TOHP-CAP

K-Number: K941031 · 1995-01-26

ApplicantJrm Ent., Inc.
Decision Date1995-01-26
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TOHP-CAP is the device name listed in this FDA 510(k) record. The listed applicant is Jrm Ent., Inc.. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K941031. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOHP-CAP?

TOHP-CAP is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Jrm Ent., Inc.. The 510(k) number is K941031.

When did TOHP-CAP receive FDA 510(k) clearance?

TOHP-CAP received FDA 510(k) clearance on 1995-01-26, under 510(k) number K941031.

Who is the listed applicant for TOHP-CAP?

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

What is the FDA product code for TOHP-CAP?

The FDA product code for TOHP-CAP is FMI.

Related Devices (Code: FMI)

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

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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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