GLOVES, APARTICULATE SURGICAL
K-Number: K760248 · 1976-08-09
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Device Summary
Frequently Asked Questions
What is the GLOVES, APARTICULATE SURGICAL?
GLOVES, APARTICULATE SURGICAL is a medical device that received FDA 510(k) clearance on 1976-08-09. The listed applicant is Deknatel, Inc.. The 510(k) number is K760248.
When did GLOVES, APARTICULATE SURGICAL receive FDA 510(k) clearance?
GLOVES, APARTICULATE SURGICAL received FDA 510(k) clearance on 1976-08-09, under 510(k) number K760248.
Who is the listed applicant for GLOVES, APARTICULATE SURGICAL?
The FDA 510(k) record lists Deknatel, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOVES, APARTICULATE SURGICAL?
The FDA product code for GLOVES, APARTICULATE SURGICAL 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 Deknatel, 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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