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FDA 510(k)

COMFORTRAC TABLE MODEL CT-1000

K-Number: K901971 · 1990-07-25

Decision Date1990-07-25
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COMFORTRAC TABLE MODEL CT-1000 is the device name listed in this FDA 510(k) record. The listed applicant is Comfortrac Systems. It received FDA 510(k) clearance on 1990-07-25 under 510(k) number K901971. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMFORTRAC TABLE MODEL CT-1000?

COMFORTRAC TABLE MODEL CT-1000 is a medical device that received FDA 510(k) clearance on 1990-07-25. The listed applicant is Comfortrac Systems. The 510(k) number is K901971.

When did COMFORTRAC TABLE MODEL CT-1000 receive FDA 510(k) clearance?

COMFORTRAC TABLE MODEL CT-1000 received FDA 510(k) clearance on 1990-07-25, under 510(k) number K901971.

Who is the listed applicant for COMFORTRAC TABLE MODEL CT-1000?

The FDA 510(k) record lists Comfortrac Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COMFORTRAC TABLE MODEL CT-1000?

The FDA product code for COMFORTRAC TABLE MODEL CT-1000 is JFB.

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 Comfortrac Systems 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: JFB)

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

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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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