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FDA 510(k)

MONITOR, PATIENT, MODEL PM-I0N

K-Number: K770968 · 1977-06-08

ApplicantCavitron Corp.
Decision Date1977-06-08
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONITOR, PATIENT, MODEL PM-I0N is the device name listed in this FDA 510(k) record. The listed applicant is Cavitron Corp.. It received FDA 510(k) clearance on 1977-06-08 under 510(k) number K770968. 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 MONITOR, PATIENT, MODEL PM-I0N?

MONITOR, PATIENT, MODEL PM-I0N is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Cavitron Corp.. The 510(k) number is K770968.

When did MONITOR, PATIENT, MODEL PM-I0N receive FDA 510(k) clearance?

MONITOR, PATIENT, MODEL PM-I0N received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770968.

Who is the listed applicant for MONITOR, PATIENT, MODEL PM-I0N?

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

What is the FDA product code for MONITOR, PATIENT, MODEL PM-I0N?

The FDA product code for MONITOR, PATIENT, MODEL PM-I0N is CCK.

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Other records listing Cavitron Corp. 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.

K811582THE PLACERK810207MINOR SURGERY LIGHTK802928SPIROMETRIC COMPUTER #SC-10K801623CAVITRON ULTRASONIC SURG. ASPIR. CUSAK801877SLIT LAMP ATTACHMENTK800869MODEL PM-20(N)(R)CO2 PATIENT MONITOR/ALA

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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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