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FDA 510(k)

SILKAFIX ADHESIVE PLASTER

K-Number: K821490 · 1982-06-02

ApplicantSelomas, Inc.
Decision Date1982-06-02
Product CodeKGX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SILKAFIX ADHESIVE PLASTER is the device name listed in this FDA 510(k) record. The listed applicant is Selomas, Inc.. It received FDA 510(k) clearance on 1982-06-02 under 510(k) number K821490. The device is classified under product code KGX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILKAFIX ADHESIVE PLASTER?

SILKAFIX ADHESIVE PLASTER is a medical device that received FDA 510(k) clearance on 1982-06-02. The listed applicant is Selomas, Inc.. The 510(k) number is K821490.

When did SILKAFIX ADHESIVE PLASTER receive FDA 510(k) clearance?

SILKAFIX ADHESIVE PLASTER received FDA 510(k) clearance on 1982-06-02, under 510(k) number K821490.

Who is the listed applicant for SILKAFIX ADHESIVE PLASTER?

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

What is the FDA product code for SILKAFIX ADHESIVE PLASTER?

The FDA product code for SILKAFIX ADHESIVE PLASTER is KGX.

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 Selomas, 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.

View all 7 devices →

Related Devices (Code: KGX)

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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