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FDA 510(k)

TENDER TOUCH SILICONE GEL PADS

K-Number: K991478 · 1999-06-21

Decision Date1999-06-21
Product CodeMDA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TENDER TOUCH SILICONE GEL PADS 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 1999-06-21 under 510(k) number K991478. 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 TENDER TOUCH SILICONE GEL PADS?

TENDER TOUCH SILICONE GEL PADS is a medical device that received FDA 510(k) clearance on 1999-06-21. The listed applicant is Capital Marketing Technologies, Inc.. The 510(k) number is K991478.

When did TENDER TOUCH SILICONE GEL PADS receive FDA 510(k) clearance?

TENDER TOUCH SILICONE GEL PADS received FDA 510(k) clearance on 1999-06-21, under 510(k) number K991478.

Who is the listed applicant for TENDER TOUCH SILICONE GEL PADS?

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 TENDER TOUCH SILICONE GEL PADS?

The FDA product code for TENDER TOUCH SILICONE GEL PADS 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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