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FDA 510(k)

CAPNOMETER MODEL 47210A

K-Number: K780324 · 1978-03-14

ApplicantHewlett-Packard Co.
Decision Date1978-03-14
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPNOMETER MODEL 47210A is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1978-03-14 under 510(k) number K780324. 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 CAPNOMETER MODEL 47210A?

CAPNOMETER MODEL 47210A is a medical device that received FDA 510(k) clearance on 1978-03-14. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K780324.

When did CAPNOMETER MODEL 47210A receive FDA 510(k) clearance?

CAPNOMETER MODEL 47210A received FDA 510(k) clearance on 1978-03-14, under 510(k) number K780324.

Who is the listed applicant for CAPNOMETER MODEL 47210A?

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

What is the FDA product code for CAPNOMETER MODEL 47210A?

The FDA product code for CAPNOMETER MODEL 47210A is CCK.

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Other records listing Hewlett-Packard Co. 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.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, Inc.

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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