RHYNOSTAT H-12 & V-22
K-Number: K852349 · 1985-09-03
Advertisement
Device Summary
Frequently Asked Questions
What is the RHYNOSTAT H-12 & V-22?
RHYNOSTAT H-12 & V-22 is a medical device that received FDA 510(k) clearance on 1985-09-03. The listed applicant is Remesta Medical Corp.. The 510(k) number is K852349.
When did RHYNOSTAT H-12 & V-22 receive FDA 510(k) clearance?
RHYNOSTAT H-12 & V-22 received FDA 510(k) clearance on 1985-09-03, under 510(k) number K852349.
Who is the listed applicant for RHYNOSTAT H-12 & V-22?
The FDA 510(k) record lists Remesta Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RHYNOSTAT H-12 & V-22?
The FDA product code for RHYNOSTAT H-12 & V-22 is KPR.
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.
Related Devices (Code: KPR)
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