FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES
K-Number: K912022 · 1991-08-02
Advertisement
Device Summary
Frequently Asked Questions
What is the FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES?
FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES is a medical device that received FDA 510(k) clearance on 1991-08-02. The listed applicant is Fraass Survival Systems, Inc.. The 510(k) number is K912022.
When did FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES receive FDA 510(k) clearance?
FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES received FDA 510(k) clearance on 1991-08-02, under 510(k) number K912022.
Who is the listed applicant for FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES?
The FDA 510(k) record lists Fraass Survival Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES?
The FDA product code for FRASTEC DRYNET, BRIDAL VEIL, VARIOUS SIZES is NAD.
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 Fraass Survival Systems, 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: NAD)
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.
Advertisement