NATURAL-TOUCH (TM) SURGEON'S GLOVE
K-Number: K872996 · 1988-03-04
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Device Summary
Frequently Asked Questions
What is the NATURAL-TOUCH (TM) SURGEON'S GLOVE?
NATURAL-TOUCH (TM) SURGEON'S GLOVE is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Hands-On Packaging , Ltd.. The 510(k) number is K872996.
When did NATURAL-TOUCH (TM) SURGEON'S GLOVE receive FDA 510(k) clearance?
NATURAL-TOUCH (TM) SURGEON'S GLOVE received FDA 510(k) clearance on 1988-03-04, under 510(k) number K872996.
Who is the listed applicant for NATURAL-TOUCH (TM) SURGEON'S GLOVE?
The FDA 510(k) record lists Hands-On Packaging , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NATURAL-TOUCH (TM) SURGEON'S GLOVE?
The FDA product code for NATURAL-TOUCH (TM) SURGEON'S GLOVE 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 Hands-On Packaging , Ltd. 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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