GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST
K-Number: K914913 · 1991-12-31
Advertisement
Device Summary
Frequently Asked Questions
What is the GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST?
GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST is a medical device that received FDA 510(k) clearance on 1991-12-31. The listed applicant is Ideal Medical, Inc.. The 510(k) number is K914913.
When did GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST receive FDA 510(k) clearance?
GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST received FDA 510(k) clearance on 1991-12-31, under 510(k) number K914913.
Who is the listed applicant for GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST?
The FDA 510(k) record lists Ideal Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST?
The FDA product code for GRICE FOOT PEDAL CONTROL/REDDICK IRRI/ASPIR SYST is GDJ.
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 Ideal Medical, Inc. 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: GDJ)
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