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FDA 510(k)

OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL

K-Number: K073310 · 2008-01-18

Decision Date2008-01-18
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL is the device name listed in this FDA 510(k) record. The listed applicant is Hitachi Medical Corp.. It received FDA 510(k) clearance on 2008-01-18 under 510(k) number K073310. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL?

OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL is a medical device that received FDA 510(k) clearance on 2008-01-18. The listed applicant is Hitachi Medical Corp.. The 510(k) number is K073310.

When did OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL receive FDA 510(k) clearance?

OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL received FDA 510(k) clearance on 2008-01-18, under 510(k) number K073310.

Who is the listed applicant for OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL?

The FDA 510(k) record lists Hitachi Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT COIL?

The FDA product code for OASIS CTL COIL, OD FLEXIBLE BODY COIL (L AND XL), AND RAPID FOOT 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 Hitachi Medical Corp. 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.

View all 11 devices →

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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