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FDA 510(k)

SKIN SUPPORT PREP PAD

K-Number: K923351 · 1992-09-14

ApplicantColoplast Corp.
Decision Date1992-09-14
Product CodeKOX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKIN SUPPORT PREP PAD is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast Corp.. It received FDA 510(k) clearance on 1992-09-14 under 510(k) number K923351. The device is classified under product code KOX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN SUPPORT PREP PAD?

SKIN SUPPORT PREP PAD is a medical device that received FDA 510(k) clearance on 1992-09-14. The listed applicant is Coloplast Corp.. The 510(k) number is K923351.

When did SKIN SUPPORT PREP PAD receive FDA 510(k) clearance?

SKIN SUPPORT PREP PAD received FDA 510(k) clearance on 1992-09-14, under 510(k) number K923351.

Who is the listed applicant for SKIN SUPPORT PREP PAD?

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

What is the FDA product code for SKIN SUPPORT PREP PAD?

The FDA product code for SKIN SUPPORT PREP PAD is KOX.

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Related Devices (Code: KOX)

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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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