LAC-MAC INNERBLOC LR SURGICAL GOWNS
K-Number: K092344 · 2009-12-17
Advertisement
Device Summary
Frequently Asked Questions
What is the LAC-MAC INNERBLOC LR SURGICAL GOWNS?
LAC-MAC INNERBLOC LR SURGICAL GOWNS is a medical device that received FDA 510(k) clearance on 2009-12-17. The listed applicant is Lac Mac, Ltd.. The 510(k) number is K092344.
When did LAC-MAC INNERBLOC LR SURGICAL GOWNS receive FDA 510(k) clearance?
LAC-MAC INNERBLOC LR SURGICAL GOWNS received FDA 510(k) clearance on 2009-12-17, under 510(k) number K092344.
Who is the listed applicant for LAC-MAC INNERBLOC LR SURGICAL GOWNS?
The FDA 510(k) record lists Lac Mac, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAC-MAC INNERBLOC LR SURGICAL GOWNS?
The FDA product code for LAC-MAC INNERBLOC LR SURGICAL GOWNS is FYA.
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 Lac Mac, Ltd. 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: FYA)
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