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FDA 510(k)

RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR

K-Number: K941252 · 1995-09-20

ApplicantAnsar
Decision Date1995-09-20
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Ansar. It received FDA 510(k) clearance on 1995-09-20 under 510(k) number K941252. 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 RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR?

RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR is a medical device that received FDA 510(k) clearance on 1995-09-20. The listed applicant is Ansar. The 510(k) number is K941252.

When did RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR receive FDA 510(k) clearance?

RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR received FDA 510(k) clearance on 1995-09-20, under 510(k) number K941252.

Who is the listed applicant for RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR?

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

What is the FDA product code for RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR?

The FDA product code for RESPIRATORY AND CARDIAC SPECTRAL FREQUENCY SIGNAL PROCESSOR is DRT.

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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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