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FDA 510(k)

AEROBITRON III

K-Number: K792121 · 1979-11-15

ApplicantStanford Scientific, Inc.
Decision Date1979-11-15
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

AEROBITRON III is the device name listed in this FDA 510(k) record. The listed applicant is Stanford Scientific, Inc.. It received FDA 510(k) clearance on 1979-11-15 under 510(k) number K792121. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AEROBITRON III?

AEROBITRON III is a medical device that received FDA 510(k) clearance on 1979-11-15. The listed applicant is Stanford Scientific, Inc.. The 510(k) number is K792121.

When did AEROBITRON III receive FDA 510(k) clearance?

AEROBITRON III received FDA 510(k) clearance on 1979-11-15, under 510(k) number K792121.

Who is the listed applicant for AEROBITRON III?

The FDA 510(k) record lists Stanford Scientific, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AEROBITRON III?

The FDA product code for AEROBITRON III is ISD.

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.

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Other records listing Stanford Scientific, 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.

K792122CHRONAEROBIC (CA-1)K792120AEROBITRON IIK791966AEROBITRON 1

Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, Inc.

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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