MDT/CASTLE 2000 SURGICAL LIGHTS
K-Number: K914076 · 1991-11-13
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Device Summary
Frequently Asked Questions
What is the MDT/CASTLE 2000 SURGICAL LIGHTS?
MDT/CASTLE 2000 SURGICAL LIGHTS is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K914076.
When did MDT/CASTLE 2000 SURGICAL LIGHTS receive FDA 510(k) clearance?
MDT/CASTLE 2000 SURGICAL LIGHTS received FDA 510(k) clearance on 1991-11-13, under 510(k) number K914076.
Who is the listed applicant for MDT/CASTLE 2000 SURGICAL LIGHTS?
The FDA 510(k) record lists Mdt Corp., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MDT/CASTLE 2000 SURGICAL LIGHTS?
The FDA product code for MDT/CASTLE 2000 SURGICAL LIGHTS is FSY.
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 Mdt Corp., 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.
Related Devices (Code: FSY)
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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