MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000
K-Number: K882323 · 1988-06-30
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Device Summary
Frequently Asked Questions
What is the MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000?
MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000 is a medical device that received FDA 510(k) clearance on 1988-06-30. The listed applicant is Meicor, Inc.. The 510(k) number is K882323.
When did MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000 receive FDA 510(k) clearance?
MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000 received FDA 510(k) clearance on 1988-06-30, under 510(k) number K882323.
Who is the listed applicant for MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000?
The FDA 510(k) record lists Meicor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000?
The FDA product code for MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000 is ITY.
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.
Related Devices (Code: ITY)
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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