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FDA 510(k)

FIRST TOUCH/VILEDON NON-WOVEN FILTER

K-Number: K915752 · 1992-09-17

Decision Date1992-09-17
Product CodeFMZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FIRST TOUCH/VILEDON NON-WOVEN FILTER is the device name listed in this FDA 510(k) record. The listed applicant is First Touch Disposables, Inc.. It received FDA 510(k) clearance on 1992-09-17 under 510(k) number K915752. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIRST TOUCH/VILEDON NON-WOVEN FILTER?

FIRST TOUCH/VILEDON NON-WOVEN FILTER is a medical device that received FDA 510(k) clearance on 1992-09-17. The listed applicant is First Touch Disposables, Inc.. The 510(k) number is K915752.

When did FIRST TOUCH/VILEDON NON-WOVEN FILTER receive FDA 510(k) clearance?

FIRST TOUCH/VILEDON NON-WOVEN FILTER received FDA 510(k) clearance on 1992-09-17, under 510(k) number K915752.

Who is the listed applicant for FIRST TOUCH/VILEDON NON-WOVEN FILTER?

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

What is the FDA product code for FIRST TOUCH/VILEDON NON-WOVEN FILTER?

The FDA product code for FIRST TOUCH/VILEDON NON-WOVEN FILTER is FMZ.

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 First Touch Disposables, 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: FMZ)

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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