RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES
K-Number: K885211 · 1989-06-13
Advertisement
Device Summary
Frequently Asked Questions
What is the RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES?
RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES is a medical device that received FDA 510(k) clearance on 1989-06-13. The listed applicant is Rf Design Assoc., Inc.. The 510(k) number is K885211.
When did RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES receive FDA 510(k) clearance?
RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES received FDA 510(k) clearance on 1989-06-13, under 510(k) number K885211.
Who is the listed applicant for RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES?
The FDA 510(k) record lists Rf Design Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES?
The FDA product code for RF-100 MONITOR, RF-P-2.5, RF-P-5, RF-P-7.5 PROBES is IYN.
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: IYN)
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