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FDA 510(k)

A-BEC 14

K-Number: K865006 · 1987-02-06

ApplicantA-Bec Mobility, Inc.
Decision Date1987-02-06
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

A-BEC 14 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 K865006. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-BEC 14?

A-BEC 14 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 K865006.

When did A-BEC 14 receive FDA 510(k) clearance?

A-BEC 14 received FDA 510(k) clearance on 1987-02-06, under 510(k) number K865006.

Who is the listed applicant for A-BEC 14?

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 A-BEC 14?

The FDA product code for A-BEC 14 is ITI.

Other records listing A-Bec Mobility, Inc. as applicant

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Related Devices (Code: ITI)

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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