PATIENT EXAMINATION GLOVE
K-Number: K915842 · 1992-04-14
Advertisement
Device Summary
Frequently Asked Questions
What is the PATIENT EXAMINATION GLOVE?
PATIENT EXAMINATION GLOVE is a medical device that received FDA 510(k) clearance on 1992-04-14. The listed applicant is Precious Mountain Ent. Corp.. The 510(k) number is K915842.
When did PATIENT EXAMINATION GLOVE receive FDA 510(k) clearance?
PATIENT EXAMINATION GLOVE received FDA 510(k) clearance on 1992-04-14, under 510(k) number K915842.
Who is the listed applicant for PATIENT EXAMINATION GLOVE?
The FDA 510(k) record lists Precious Mountain Ent. Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATIENT EXAMINATION GLOVE?
The FDA product code for 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 Precious Mountain Ent. 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.
Advertisement