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FDA 510(k)

CAPNOGRAPH

K-Number: K831776 · 1983-10-31

ApplicantDatascope Corp.
Decision Date1983-10-31
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPNOGRAPH is the device name listed in this FDA 510(k) record. The listed applicant is Datascope Corp.. It received FDA 510(k) clearance on 1983-10-31 under 510(k) number K831776. 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 CAPNOGRAPH?

CAPNOGRAPH is a medical device that received FDA 510(k) clearance on 1983-10-31. The listed applicant is Datascope Corp.. The 510(k) number is K831776.

When did CAPNOGRAPH receive FDA 510(k) clearance?

CAPNOGRAPH received FDA 510(k) clearance on 1983-10-31, under 510(k) number K831776.

Who is the listed applicant for CAPNOGRAPH?

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

What is the FDA product code for CAPNOGRAPH?

The FDA product code for CAPNOGRAPH is CCK.

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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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