FDA 510(k)

STIM-8

K-Number: K955736 · 1996-05-22

Decision Date1996-05-22

Product CodeIPF

Advisory CommitteePM

DecisionSubstantially Equivalent for Some Indications

Device Summary

STIM-8 is the device name listed in this FDA 510(k) record. The listed applicant is Bmr , Ltd.. It received FDA 510(k) clearance on 1996-05-22 under 510(k) number K955736. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the STIM-8?

STIM-8 is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Bmr , Ltd.. The 510(k) number is K955736.

When did STIM-8 receive FDA 510(k) clearance?

STIM-8 received FDA 510(k) clearance on 1996-05-22, under 510(k) number K955736.

Who is the listed applicant for STIM-8?

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

What is the FDA product code for STIM-8?

The FDA product code for STIM-8 is IPF.

Related Devices (Code: IPF)

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.