ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE
K-Number: K960247 · 1996-07-29
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Device Summary
Frequently Asked Questions
What is the ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE?
ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1996-07-29. The listed applicant is Tillotson Healthcare Corp.. The 510(k) number is K960247.
When did ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?
ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1996-07-29, under 510(k) number K960247.
Who is the listed applicant for ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE?
The FDA 510(k) record lists Tillotson Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT EXAMINATION GLOVE?
The FDA product code for ULTRA CARE POWDER FREE HYPOALLERGENIC PATIENT 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 Tillotson Healthcare 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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