MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM
K-Number: K882595 · 1988-10-04
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Device Summary
Frequently Asked Questions
What is the MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM?
MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM is a medical device that received FDA 510(k) clearance on 1988-10-04. The listed applicant is Marathon Management Co.. The 510(k) number is K882595.
When did MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM receive FDA 510(k) clearance?
MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM received FDA 510(k) clearance on 1988-10-04, under 510(k) number K882595.
Who is the listed applicant for MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM?
The FDA 510(k) record lists Marathon Management Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM?
The FDA product code for MEDICAL GLOVES STERILE LATEX SURGEONS DIGIFORM 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.
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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