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FDA 510(k)

PREVENT I

K-Number: K973373 · 1998-02-26

Decision Date1998-02-26
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PREVENT I is the device name listed in this FDA 510(k) record. The listed applicant is The Buzzz Corp.. It received FDA 510(k) clearance on 1998-02-26 under 510(k) number K973373. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREVENT I?

PREVENT I is a medical device that received FDA 510(k) clearance on 1998-02-26. The listed applicant is The Buzzz Corp.. The 510(k) number is K973373.

When did PREVENT I receive FDA 510(k) clearance?

PREVENT I received FDA 510(k) clearance on 1998-02-26, under 510(k) number K973373.

Who is the listed applicant for PREVENT I?

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

What is the FDA product code for PREVENT I?

The FDA product code for PREVENT I is INO.

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 The Buzzz 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.

Related Devices (Code: INO)

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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