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FDA 510(k)

PORTABLE INTENSIVE CARE UNIT, MODEL PIC

K-Number: K000712 · 2000-04-27

ApplicantMedical Research Laboratories, Inc.
Decision Date2000-04-27
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PORTABLE INTENSIVE CARE UNIT, MODEL PIC is the device name listed in this FDA 510(k) record. The listed applicant is Medical Research Laboratories, Inc.. It received FDA 510(k) clearance on 2000-04-27 under 510(k) number K000712. 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 PORTABLE INTENSIVE CARE UNIT, MODEL PIC?

PORTABLE INTENSIVE CARE UNIT, MODEL PIC is a medical device that received FDA 510(k) clearance on 2000-04-27. The listed applicant is Medical Research Laboratories, Inc.. The 510(k) number is K000712.

When did PORTABLE INTENSIVE CARE UNIT, MODEL PIC receive FDA 510(k) clearance?

PORTABLE INTENSIVE CARE UNIT, MODEL PIC received FDA 510(k) clearance on 2000-04-27, under 510(k) number K000712.

Who is the listed applicant for PORTABLE INTENSIVE CARE UNIT, MODEL PIC?

The FDA 510(k) record lists Medical Research Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE INTENSIVE CARE UNIT, MODEL PIC?

The FDA product code for PORTABLE INTENSIVE CARE UNIT, MODEL PIC is CCK.

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Other records listing Medical Research Laboratories, Inc. 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.

K021168JUMP START, MODEL 970300K012766PORTABLE INTENSIVE CARE UNITK012030PORTABLE INTENSIVE CARE UNITK010207PORTABLE INSTENSIVE CARE UNITK002232AEDEFIBRILLATORK983307MODIFICATION TO PORTABLE INTENSIVE CARE UNIT

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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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