ENDICOTT & BEAMAN SUPRA-TEC FACE MASK
K-Number: K881372 · 1988-04-08
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Device Summary
Frequently Asked Questions
What is the ENDICOTT & BEAMAN SUPRA-TEC FACE MASK?
ENDICOTT & BEAMAN SUPRA-TEC FACE MASK is a medical device that received FDA 510(k) clearance on 1988-04-08. The listed applicant is Endicott & Beaman, Inc.. The 510(k) number is K881372.
When did ENDICOTT & BEAMAN SUPRA-TEC FACE MASK receive FDA 510(k) clearance?
ENDICOTT & BEAMAN SUPRA-TEC FACE MASK received FDA 510(k) clearance on 1988-04-08, under 510(k) number K881372.
Who is the listed applicant for ENDICOTT & BEAMAN SUPRA-TEC FACE MASK?
The FDA 510(k) record lists Endicott & Beaman, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDICOTT & BEAMAN SUPRA-TEC FACE MASK?
The FDA product code for ENDICOTT & BEAMAN SUPRA-TEC FACE MASK is FXX.
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.
Related Devices (Code: FXX)
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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