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FDA 510(k)

HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103

K-Number: K021622 · 2003-04-01

Decision Date2003-04-01
Product CodeMQM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103 is the device name listed in this FDA 510(k) record. The listed applicant is Hill-Rom Air-Shields. It received FDA 510(k) clearance on 2003-04-01 under 510(k) number K021622. The device is classified under product code MQM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103?

HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103 is a medical device that received FDA 510(k) clearance on 2003-04-01. The listed applicant is Hill-Rom Air-Shields. The 510(k) number is K021622.

When did HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103 receive FDA 510(k) clearance?

HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103 received FDA 510(k) clearance on 2003-04-01, under 510(k) number K021622.

Who is the listed applicant for HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103?

The FDA 510(k) record lists Hill-Rom Air-Shields as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103?

The FDA product code for HILL-ROM AIR SHIELDS/MINOLTA JAUNDICE METER, MODEL JM-103 is MQM.

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 Hill-Rom Air-Shields 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.

Related Devices (Code: MQM)

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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