SEAMLESS LATEX PATIENT EXAMINATION GLOVES
K-Number: K891491 · 1989-05-08
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Device Summary
Frequently Asked Questions
What is the SEAMLESS LATEX PATIENT EXAMINATION GLOVES?
SEAMLESS LATEX PATIENT EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-05-08. The listed applicant is Digitcare Corp.. The 510(k) number is K891491.
When did SEAMLESS LATEX PATIENT EXAMINATION GLOVES receive FDA 510(k) clearance?
SEAMLESS LATEX PATIENT EXAMINATION GLOVES received FDA 510(k) clearance on 1989-05-08, under 510(k) number K891491.
Who is the listed applicant for SEAMLESS LATEX PATIENT EXAMINATION GLOVES?
The FDA 510(k) record lists Digitcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEAMLESS LATEX PATIENT EXAMINATION GLOVES?
The FDA product code for SEAMLESS LATEX PATIENT EXAMINATION GLOVES is LYY.
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 Digitcare 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: LYY)
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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