PELVIC ARRAY COIL
K-Number: K033753 · 2003-12-17
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Device Summary
Frequently Asked Questions
What is the PELVIC ARRAY COIL?
PELVIC ARRAY COIL is a medical device that received FDA 510(k) clearance on 2003-12-17. The listed applicant is Usa Instruments, Inc.. The 510(k) number is K033753.
When did PELVIC ARRAY COIL receive FDA 510(k) clearance?
PELVIC ARRAY COIL received FDA 510(k) clearance on 2003-12-17, under 510(k) number K033753.
Who is the listed applicant for PELVIC ARRAY COIL?
The FDA 510(k) record lists Usa Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PELVIC ARRAY COIL?
The FDA product code for PELVIC ARRAY COIL 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 Usa Instruments, 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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