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FDA 510(k)

SIMPLICARE TRANSPARENT WOUND DRESSING

K-Number: K991214 · 1999-10-14

Decision Date1999-10-14
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

SIMPLICARE TRANSPARENT WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1999-10-14 under 510(k) number K991214. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPLICARE TRANSPARENT WOUND DRESSING?

SIMPLICARE TRANSPARENT WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1999-10-14. The listed applicant is Hollister, Inc.. The 510(k) number is K991214.

When did SIMPLICARE TRANSPARENT WOUND DRESSING receive FDA 510(k) clearance?

SIMPLICARE TRANSPARENT WOUND DRESSING received FDA 510(k) clearance on 1999-10-14, under 510(k) number K991214.

Who is the listed applicant for SIMPLICARE TRANSPARENT WOUND DRESSING?

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

What is the FDA product code for SIMPLICARE TRANSPARENT WOUND DRESSING?

The FDA product code for SIMPLICARE TRANSPARENT WOUND 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 Hollister, Inc. 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.

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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

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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