ALMATEX PATIENT EXAMINATION GLOVES (LATEX)
K-Number: K891748 · 1989-05-12
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Device Summary
Frequently Asked Questions
What is the ALMATEX PATIENT EXAMINATION GLOVES (LATEX)?
ALMATEX PATIENT EXAMINATION GLOVES (LATEX) is a medical device that received FDA 510(k) clearance on 1989-05-12. The listed applicant is Healthgard Medical Products Ltd. Partnership. The 510(k) number is K891748.
When did ALMATEX PATIENT EXAMINATION GLOVES (LATEX) receive FDA 510(k) clearance?
ALMATEX PATIENT EXAMINATION GLOVES (LATEX) received FDA 510(k) clearance on 1989-05-12, under 510(k) number K891748.
Who is the listed applicant for ALMATEX PATIENT EXAMINATION GLOVES (LATEX)?
The FDA 510(k) record lists Healthgard Medical Products Ltd. Partnership as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALMATEX PATIENT EXAMINATION GLOVES (LATEX)?
The FDA product code for ALMATEX PATIENT EXAMINATION GLOVES (LATEX) 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 Healthgard Medical Products Ltd. Partnership 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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