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FDA 510(k)

POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING

K-Number: K942774 · 1994-07-20

Decision Date1994-07-20
Product CodeMGP
DecisionSubstantially Equivalent for Some Indications

Device Summary

POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is The Kendal Co.. It received FDA 510(k) clearance on 1994-07-20 under 510(k) number K942774. The device is classified under product code MGP. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING?

POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING is a medical device that received FDA 510(k) clearance on 1994-07-20. The listed applicant is The Kendal Co.. The 510(k) number is K942774.

When did POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING receive FDA 510(k) clearance?

POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING received FDA 510(k) clearance on 1994-07-20, under 510(k) number K942774.

Who is the listed applicant for POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING?

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

What is the FDA product code for POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING?

The FDA product code for POLYSKIN(R) M.R. MOIST RESPONSIVE TRANSPARENT DRESSING is MGP.

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.

Other records listing The Kendal Co. as applicant

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.

View all 63 devices →

Related Devices (Code: MGP)

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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