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FDA 510(k)

MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT

K-Number: K931197 · 1993-09-23

Decision Date1993-09-23
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Meddev International Corp.. It received FDA 510(k) clearance on 1993-09-23 under 510(k) number K931197. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT?

MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT is a medical device that received FDA 510(k) clearance on 1993-09-23. The listed applicant is Meddev International Corp.. The 510(k) number is K931197.

When did MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT receive FDA 510(k) clearance?

MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT received FDA 510(k) clearance on 1993-09-23, under 510(k) number K931197.

Who is the listed applicant for MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT?

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

What is the FDA product code for MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT?

The FDA product code for MEDDEV MULTARRAY (TM) MEDICAL EXAMINATION LIGHT is KZF.

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 Meddev International 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.

Related Devices (Code: KZF)

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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