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FDA 510(k)

NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM

K-Number: K942227 · 1996-06-28

ApplicantC.L. Mcintosh & Assoc., Inc.
Decision Date1996-06-28
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is C.L. Mcintosh & Assoc., Inc.. It received FDA 510(k) clearance on 1996-06-28 under 510(k) number K942227. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM?

NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM is a medical device that received FDA 510(k) clearance on 1996-06-28. The listed applicant is C.L. Mcintosh & Assoc., Inc.. The 510(k) number is K942227.

When did NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM receive FDA 510(k) clearance?

NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM received FDA 510(k) clearance on 1996-06-28, under 510(k) number K942227.

Who is the listed applicant for NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM?

The FDA 510(k) record lists C.L. Mcintosh & Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM?

The FDA product code for NICAS 2001 NONINVASIVE CARDIO-RESPIRATORY SYSTEM is DSB.

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Other records listing C.L. Mcintosh & Assoc., Inc. as applicant

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Related Devices (Code: DSB)

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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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