CHAMP-PAQ LATEX PATIENT EXAM GLOVES
K-Number: K892243 · 1989-08-21
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Device Summary
Frequently Asked Questions
What is the CHAMP-PAQ LATEX PATIENT EXAM GLOVES?
CHAMP-PAQ LATEX PATIENT EXAM GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Champ-Paq Instrument Corp.. The 510(k) number is K892243.
When did CHAMP-PAQ LATEX PATIENT EXAM GLOVES receive FDA 510(k) clearance?
CHAMP-PAQ LATEX PATIENT EXAM GLOVES received FDA 510(k) clearance on 1989-08-21, under 510(k) number K892243.
Who is the listed applicant for CHAMP-PAQ LATEX PATIENT EXAM GLOVES?
The FDA 510(k) record lists Champ-Paq Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHAMP-PAQ LATEX PATIENT EXAM GLOVES?
The FDA product code for CHAMP-PAQ LATEX PATIENT EXAM 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 Champ-Paq Instrument 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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