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FDA 510(k)

MULTICURE(R) S GEL PAD

K-Number: K950085 · 1995-07-13

Decision Date1995-07-13
Product CodeKIC
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTICURE(R) S GEL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Multigestion (Deutschland) GmbH. It received FDA 510(k) clearance on 1995-07-13 under 510(k) number K950085. The device is classified under product code KIC. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTICURE(R) S GEL PAD?

MULTICURE(R) S GEL PAD is a medical device that received FDA 510(k) clearance on 1995-07-13. The listed applicant is Multigestion (Deutschland) GmbH. The 510(k) number is K950085.

When did MULTICURE(R) S GEL PAD receive FDA 510(k) clearance?

MULTICURE(R) S GEL PAD received FDA 510(k) clearance on 1995-07-13, under 510(k) number K950085.

Who is the listed applicant for MULTICURE(R) S GEL PAD?

The FDA 510(k) record lists Multigestion (Deutschland) GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTICURE(R) S GEL PAD?

The FDA product code for MULTICURE(R) S GEL PAD is KIC.

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.

Related Devices (Code: KIC)

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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