LINEAR SHOULDER COIL, MODEL 414GE-09
K-Number: K991115 · 1999-06-08
Advertisement
Device Summary
Frequently Asked Questions
What is the LINEAR SHOULDER COIL, MODEL 414GE-09?
LINEAR SHOULDER COIL, MODEL 414GE-09 is a medical device that received FDA 510(k) clearance on 1999-06-08. The listed applicant is Medical Advances, Inc.. The 510(k) number is K991115.
When did LINEAR SHOULDER COIL, MODEL 414GE-09 receive FDA 510(k) clearance?
LINEAR SHOULDER COIL, MODEL 414GE-09 received FDA 510(k) clearance on 1999-06-08, under 510(k) number K991115.
Who is the listed applicant for LINEAR SHOULDER COIL, MODEL 414GE-09?
The FDA 510(k) record lists Medical Advances, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LINEAR SHOULDER COIL, MODEL 414GE-09?
The FDA product code for LINEAR SHOULDER COIL, MODEL 414GE-09 is MOS.
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 Medical Advances, 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: MOS)
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