MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES
K-Number: K000345 · 2000-04-11
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Device Summary
Frequently Asked Questions
What is the MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES?
MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES is a medical device that received FDA 510(k) clearance on 2000-04-11. The listed applicant is Medical Advances, Inc.. The 510(k) number is K000345.
When did MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES receive FDA 510(k) clearance?
MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES received FDA 510(k) clearance on 2000-04-11, under 510(k) number K000345.
Who is the listed applicant for MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES?
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 MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES?
The FDA product code for MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES 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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