MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION
K-Number: K940284 · 1994-02-28
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Device Summary
Frequently Asked Questions
What is the MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION?
MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-02-28. The listed applicant is Meddev International Corp.. The 510(k) number is K940284.
When did MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION receive FDA 510(k) clearance?
MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION received FDA 510(k) clearance on 1994-02-28, under 510(k) number K940284.
Who is the listed applicant for MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION?
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 MEDICAL EXAMINING LIGHT MODIFICATION?
The FDA product code for MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATION 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
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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