PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES)
K-Number: K892101 · 1989-05-08
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Device Summary
Frequently Asked Questions
What is the PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES)?
PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES) is a medical device that received FDA 510(k) clearance on 1989-05-08. The listed applicant is Ergo Intl., Ent., Inc.. The 510(k) number is K892101.
When did PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES) receive FDA 510(k) clearance?
PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES) received FDA 510(k) clearance on 1989-05-08, under 510(k) number K892101.
Who is the listed applicant for PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES)?
The FDA 510(k) record lists Ergo Intl., Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER GLOVES)?
The FDA product code for PATIENT EXAM GLOVES (MFG. SHUN TAHI RUBBER 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 Ergo Intl., Ent., 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: 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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