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FDA 510(k)

FORMOSTAR

K-Number: K862106 · 1986-08-21

ApplicantLmv, Liske & Methling, GmbH
Decision Date1986-08-21
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORMOSTAR is the device name listed in this FDA 510(k) record. The listed applicant is Lmv, Liske & Methling, GmbH. It received FDA 510(k) clearance on 1986-08-21 under 510(k) number K862106. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORMOSTAR?

FORMOSTAR is a medical device that received FDA 510(k) clearance on 1986-08-21. The listed applicant is Lmv, Liske & Methling, GmbH. The 510(k) number is K862106.

When did FORMOSTAR receive FDA 510(k) clearance?

FORMOSTAR received FDA 510(k) clearance on 1986-08-21, under 510(k) number K862106.

Who is the listed applicant for FORMOSTAR?

The FDA 510(k) record lists Lmv, Liske & Methling, GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORMOSTAR?

The FDA product code for FORMOSTAR is IRT.

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Related Devices (Code: IRT)

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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