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FDA 510(k)

CAPNOMETER W/NEW AIRWAY ADAPTER 47210A

K-Number: K831447 · 1983-11-21

Decision Date1983-11-21
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAPNOMETER W/NEW AIRWAY ADAPTER 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 1983-11-21 under 510(k) number K831447. 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 W/NEW AIRWAY ADAPTER 47210A?

CAPNOMETER W/NEW AIRWAY ADAPTER 47210A is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K831447.

When did CAPNOMETER W/NEW AIRWAY ADAPTER 47210A receive FDA 510(k) clearance?

CAPNOMETER W/NEW AIRWAY ADAPTER 47210A received FDA 510(k) clearance on 1983-11-21, under 510(k) number K831447.

Who is the listed applicant for CAPNOMETER W/NEW AIRWAY ADAPTER 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 W/NEW AIRWAY ADAPTER 47210A?

The FDA product code for CAPNOMETER W/NEW AIRWAY ADAPTER 47210A is CCK.

Related Clinical Trials

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.

Other records listing Hewlett-Packard Co. as applicant

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.

View all 230 devices →

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.

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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