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FDA 510(k)

NORMOCAP 200 CAPNOMETER

K-Number: K882748 · 1988-10-19

ApplicantDatex Division Instrumentarium Corp.
Decision Date1988-10-19
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

NORMOCAP 200 CAPNOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Datex Division Instrumentarium Corp.. It received FDA 510(k) clearance on 1988-10-19 under 510(k) number K882748. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORMOCAP 200 CAPNOMETER?

NORMOCAP 200 CAPNOMETER is a medical device that received FDA 510(k) clearance on 1988-10-19. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K882748.

When did NORMOCAP 200 CAPNOMETER receive FDA 510(k) clearance?

NORMOCAP 200 CAPNOMETER received FDA 510(k) clearance on 1988-10-19, under 510(k) number K882748.

Who is the listed applicant for NORMOCAP 200 CAPNOMETER?

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

What is the FDA product code for NORMOCAP 200 CAPNOMETER?

The FDA product code for NORMOCAP 200 CAPNOMETER is CCK.

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Other records listing Datex Division Instrumentarium Corp. as applicant

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Related Devices (Code: CCK)

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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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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