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FDA 510(k)

SCOOTA MOTORIZED VEHICLE

K-Number: K864686 · 1986-12-16

Decision Date1986-12-16
Product CodeINI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SCOOTA 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 1986-12-16 under 510(k) number K864686. 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 MOTORIZED VEHICLE?

SCOOTA MOTORIZED VEHICLE is a medical device that received FDA 510(k) clearance on 1986-12-16. The listed applicant is A-Bec Mobility, Inc.. The 510(k) number is K864686.

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

SCOOTA MOTORIZED VEHICLE received FDA 510(k) clearance on 1986-12-16, under 510(k) number K864686.

Who is the listed applicant for SCOOTA 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 MOTORIZED VEHICLE?

The FDA product code for SCOOTA MOTORIZED VEHICLE is INI.

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 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.

View all 14 devices →

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.

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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