'MED-TECH' LATEX EXAMINATION GLOVE
K-Number: K894552 · 1989-10-31
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Device Summary
Frequently Asked Questions
What is the 'MED-TECH' LATEX EXAMINATION GLOVE?
'MED-TECH' LATEX EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is Med-Tech Rubber & Engineering Industries. The 510(k) number is K894552.
When did 'MED-TECH' LATEX EXAMINATION GLOVE receive FDA 510(k) clearance?
'MED-TECH' LATEX EXAMINATION GLOVE received FDA 510(k) clearance on 1989-10-31, under 510(k) number K894552.
Who is the listed applicant for 'MED-TECH' LATEX EXAMINATION GLOVE?
The FDA 510(k) record lists Med-Tech Rubber & Engineering Industries as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 'MED-TECH' LATEX EXAMINATION GLOVE?
The FDA product code for 'MED-TECH' LATEX EXAMINATION GLOVE 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 Med-Tech Rubber & Engineering Industries 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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