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FDA 510(k)

THE BODY BUGGY

K-Number: K915361 · 1991-12-20

ApplicantInnova Corp.
Decision Date1991-12-20
Product CodeLYG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THE BODY BUGGY is the device name listed in this FDA 510(k) record. The listed applicant is Innova Corp.. It received FDA 510(k) clearance on 1991-12-20 under 510(k) number K915361. The device is classified under product code LYG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BODY BUGGY?

THE BODY BUGGY is a medical device that received FDA 510(k) clearance on 1991-12-20. The listed applicant is Innova Corp.. The 510(k) number is K915361.

When did THE BODY BUGGY receive FDA 510(k) clearance?

THE BODY BUGGY received FDA 510(k) clearance on 1991-12-20, under 510(k) number K915361.

Who is the listed applicant for THE BODY BUGGY?

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

What is the FDA product code for THE BODY BUGGY?

The FDA product code for THE BODY BUGGY is LYG.

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 Innova 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: LYG)

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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