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FDA 510(k)

CHRONAEROBIC (CA-1)

K-Number: K792122 · 1979-11-27

ApplicantStanford Scientific, Inc.
Decision Date1979-11-27
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CHRONAEROBIC (CA-1) 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 1979-11-27 under 510(k) number K792122. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHRONAEROBIC (CA-1)?

CHRONAEROBIC (CA-1) is a medical device that received FDA 510(k) clearance on 1979-11-27. The listed applicant is Stanford Scientific, Inc.. The 510(k) number is K792122.

When did CHRONAEROBIC (CA-1) receive FDA 510(k) clearance?

CHRONAEROBIC (CA-1) received FDA 510(k) clearance on 1979-11-27, under 510(k) number K792122.

Who is the listed applicant for CHRONAEROBIC (CA-1)?

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 CHRONAEROBIC (CA-1)?

The FDA product code for CHRONAEROBIC (CA-1) is DRT.

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.

K792120AEROBITRON IIK792121AEROBITRON IIIK791966AEROBITRON 1

Related Devices (Code: DRT)

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.

K254058DistaSense(TM) (v1)Life Detection TechnologiesK261286The Circadia C300 System (C300)Circadia Health, Inc.K252676The Circadia C300 System (C300)Circadia Health, Inc.K253388Sleepiz One+ (Model 2.5)Sleepiz AGK251364Sleepiz One+ (2.5)Sleepiz AGK234003The Circadia C200 SystemCircadia Technologies, Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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