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FDA 510(k)

SCOOTA BUG (MOTORIZED VEHICLE)

K-Number: K880424 · 1988-02-16

ApplicantA-Bec Mobility, Inc.
Decision Date1988-02-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCOOTA BUG (MOTORIZED VEHICLE) is the device name listed in this FDA 510(k) record. The listed applicant is A-Bec Mobility, Inc.. It received FDA 510(k) clearance on 1988-02-16 under 510(k) number K880424. The device is classified under product code INI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOOTA BUG (MOTORIZED VEHICLE)?

SCOOTA BUG (MOTORIZED VEHICLE) is a medical device that received FDA 510(k) clearance on 1988-02-16. The listed applicant is A-Bec Mobility, Inc.. The 510(k) number is K880424.

When did SCOOTA BUG (MOTORIZED VEHICLE) receive FDA 510(k) clearance?

SCOOTA BUG (MOTORIZED VEHICLE) received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880424.

Who is the listed applicant for SCOOTA BUG (MOTORIZED VEHICLE)?

The FDA 510(k) record lists A-Bec Mobility, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCOOTA BUG (MOTORIZED VEHICLE)?

The FDA product code for SCOOTA BUG (MOTORIZED VEHICLE) is INI.

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Other records listing A-Bec Mobility, 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.

K880423TARGA (WHEELCHAIR)K880425STERLING (MOTORIZED VEHICLE)K865001A-BEC FIREBALL 40K865006A-BEC 14K865009A-BEC 47K865004A-BEC 40 POWER WHEELCHAIR

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Related Devices (Code: INI)

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.

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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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