STERLING (MOTORIZED VEHICLE)
K-Number: K880425 · 1988-02-16
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Device Summary
Frequently Asked Questions
What is the STERLING (MOTORIZED VEHICLE)?
STERLING (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 K880425.
When did STERLING (MOTORIZED VEHICLE) receive FDA 510(k) clearance?
STERLING (MOTORIZED VEHICLE) received FDA 510(k) clearance on 1988-02-16, under 510(k) number K880425.
Who is the listed applicant for STERLING (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 STERLING (MOTORIZED VEHICLE)?
The FDA product code for STERLING (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.
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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