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FDA 510(k)

NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS

K-Number: K984213 · 1999-04-14

Decision Date1999-04-14
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS is the device name listed in this FDA 510(k) record. The listed applicant is Capital Marketing Technologies, Inc.. It received FDA 510(k) clearance on 1999-04-14 under 510(k) number K984213. The device is classified under product code MDA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS?

NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS is a medical device that received FDA 510(k) clearance on 1999-04-14. The listed applicant is Capital Marketing Technologies, Inc.. The 510(k) number is K984213.

When did NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS receive FDA 510(k) clearance?

NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS received FDA 510(k) clearance on 1999-04-14, under 510(k) number K984213.

Who is the listed applicant for NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS?

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

What is the FDA product code for NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS?

The FDA product code for NEARLY ME RETOUCH SILICONE SCAR REDUCTION SHEETS is MDA.

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 Capital Marketing Technologies, 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.

Related Devices (Code: MDA)

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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