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FDA 510(k)

DERMASSIST TRANSPARENT SITE DRESSING

K-Number: K924249 · 1993-02-03

ApplicantWilshire Medical Products
Decision Date1993-02-03
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DERMASSIST TRANSPARENT SITE DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Wilshire Medical Products. It received FDA 510(k) clearance on 1993-02-03 under 510(k) number K924249. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DERMASSIST TRANSPARENT SITE DRESSING?

DERMASSIST TRANSPARENT SITE DRESSING is a medical device that received FDA 510(k) clearance on 1993-02-03. The listed applicant is Wilshire Medical Products. The 510(k) number is K924249.

When did DERMASSIST TRANSPARENT SITE DRESSING receive FDA 510(k) clearance?

DERMASSIST TRANSPARENT SITE DRESSING received FDA 510(k) clearance on 1993-02-03, under 510(k) number K924249.

Who is the listed applicant for DERMASSIST TRANSPARENT SITE DRESSING?

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

What is the FDA product code for DERMASSIST TRANSPARENT SITE DRESSING?

The FDA product code for DERMASSIST TRANSPARENT SITE DRESSING is KMK.

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Other records listing Wilshire Medical Products 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.

K946031DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSINGK946030DERMASSIST(TM) HYDROGEL SATURATED GAUZE DRESSINGK944333HYDRODERM GEL WOUND DRESSINGK941216HYDRODERM EXTRA THIN INTELLIGENT HYDROCOLLIOID DRESSINGK941149DERMAASSIST HYDROCOLLOID DRESSINGK941005DERMASSIST(TM) XEROFORM PETROLATUM DRESSING

View all 12 devices →

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, Inc.

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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