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FDA 510(k)

A-BEC 18

K-Number: K865002 · 1987-02-06

ApplicantA-Bec Mobility, Inc.
Decision Date1987-02-06
Product Code
DecisionSubstantially Equivalent

Device Summary

A-BEC 18 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 1987-02-06 under 510(k) number K865002. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-BEC 18?

A-BEC 18 is a medical device that received FDA 510(k) clearance on 1987-02-06. The listed applicant is A-Bec Mobility, Inc.. The 510(k) number is K865002.

When did A-BEC 18 receive FDA 510(k) clearance?

A-BEC 18 received FDA 510(k) clearance on 1987-02-06, under 510(k) number K865002.

Who is the listed applicant for A-BEC 18?

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

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)K880424SCOOTA BUG (MOTORIZED VEHICLE)K880425STERLING (MOTORIZED VEHICLE)K865001A-BEC FIREBALL 40K865009A-BEC 47K865006A-BEC 14

View all 14 devices →

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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