MULTICURE(R) S GEL PAD
K-Number: K950085 · 1995-07-13
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement