`INEAR WRIST COIL, MODEL 440GE-09
K-Number: K991113 · 1999-06-10
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Device Summary
Frequently Asked Questions
What is the `INEAR WRIST COIL, MODEL 440GE-09?
`INEAR WRIST COIL, MODEL 440GE-09 is a medical device that received FDA 510(k) clearance on 1999-06-10. The listed applicant is Medical Advances, Inc.. The 510(k) number is K991113.
When did `INEAR WRIST COIL, MODEL 440GE-09 receive FDA 510(k) clearance?
`INEAR WRIST COIL, MODEL 440GE-09 received FDA 510(k) clearance on 1999-06-10, under 510(k) number K991113.
Who is the listed applicant for `INEAR WRIST COIL, MODEL 440GE-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 `INEAR WRIST COIL, MODEL 440GE-09?
The FDA product code for `INEAR WRIST COIL, MODEL 440GE-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.
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