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FDA 510(k)

MEDISYSTEMS TRANSDUCER PROTECTOR

K-Number: K983076 · 1998-11-25

Decision Date1998-11-25
Product CodeFIB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MEDISYSTEMS TRANSDUCER PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Medisystems Corp.. It received FDA 510(k) clearance on 1998-11-25 under 510(k) number K983076. The device is classified under product code FIB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDISYSTEMS TRANSDUCER PROTECTOR?

MEDISYSTEMS TRANSDUCER PROTECTOR is a medical device that received FDA 510(k) clearance on 1998-11-25. The listed applicant is Medisystems Corp.. The 510(k) number is K983076.

When did MEDISYSTEMS TRANSDUCER PROTECTOR receive FDA 510(k) clearance?

MEDISYSTEMS TRANSDUCER PROTECTOR received FDA 510(k) clearance on 1998-11-25, under 510(k) number K983076.

Who is the listed applicant for MEDISYSTEMS TRANSDUCER PROTECTOR?

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

What is the FDA product code for MEDISYSTEMS TRANSDUCER PROTECTOR?

The FDA product code for MEDISYSTEMS TRANSDUCER PROTECTOR is FIB.

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 Medisystems 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 22 devices →

Related Devices (Code: FIB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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