CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER
K-Number: K920876 · 1992-12-11
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Device Summary
Frequently Asked Questions
What is the CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER?
CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER is a medical device that received FDA 510(k) clearance on 1992-12-11. The listed applicant is Medtech Intl., Inc.. The 510(k) number is K920876.
When did CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER receive FDA 510(k) clearance?
CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER received FDA 510(k) clearance on 1992-12-11, under 510(k) number K920876.
Who is the listed applicant for CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER?
The FDA 510(k) record lists Medtech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER?
The FDA product code for CUT RESISTANT GLOVES OR SURGICAL GLOVE LINER is KGO.
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 Medtech Intl., 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: KGO)
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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