GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE
K-Number: K770056 · 1977-02-25
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Device Summary
Frequently Asked Questions
What is the GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE?
GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE is a medical device that received FDA 510(k) clearance on 1977-02-25. The listed applicant is Arbrook Mfg. Corp.. The 510(k) number is K770056.
When did GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE receive FDA 510(k) clearance?
GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE received FDA 510(k) clearance on 1977-02-25, under 510(k) number K770056.
Who is the listed applicant for GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE?
The FDA 510(k) record lists Arbrook Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE?
The FDA product code for GLOVES, SURGEONS,MICRO-TOUCH POWDERFREE 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 Arbrook Mfg. Corp. 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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