RIFTON MOR219 19 & RIFTON MOR225 25
K-Number: K921817 · 1992-04-29
Advertisement
Device Summary
Frequently Asked Questions
What is the RIFTON MOR219 19 & RIFTON MOR225 25?
RIFTON MOR219 19 & RIFTON MOR225 25 is a medical device that received FDA 510(k) clearance on 1992-04-29. The listed applicant is Rifton Equipment For the Handicapped. The 510(k) number is K921817.
When did RIFTON MOR219 19 & RIFTON MOR225 25 receive FDA 510(k) clearance?
RIFTON MOR219 19 & RIFTON MOR225 25 received FDA 510(k) clearance on 1992-04-29, under 510(k) number K921817.
Who is the listed applicant for RIFTON MOR219 19 & RIFTON MOR225 25?
The FDA 510(k) record lists Rifton Equipment For the Handicapped as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIFTON MOR219 19 & RIFTON MOR225 25?
The FDA product code for RIFTON MOR219 19 & RIFTON MOR225 25 is INM.
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 Rifton Equipment For the Handicapped 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: INM)
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