DR. BOO LATEX EXAMINATION GLOVES
K-Number: K893520 · 1989-08-21
Advertisement
Device Summary
Frequently Asked Questions
What is the DR. BOO LATEX EXAMINATION GLOVES?
DR. BOO LATEX EXAMINATION GLOVES is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Dynatech Medical Products. The 510(k) number is K893520.
When did DR. BOO LATEX EXAMINATION GLOVES receive FDA 510(k) clearance?
DR. BOO LATEX EXAMINATION GLOVES received FDA 510(k) clearance on 1989-08-21, under 510(k) number K893520.
Who is the listed applicant for DR. BOO LATEX EXAMINATION GLOVES?
The FDA 510(k) record lists Dynatech Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DR. BOO LATEX EXAMINATION GLOVES?
The FDA product code for DR. BOO LATEX EXAMINATION 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 Dynatech Medical Products 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