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FDA 510(k)

MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000

K-Number: K882323 · 1988-06-30

ApplicantMeicor, Inc.
Decision Date1988-06-30
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEICOR X-RAY TUBE, MODELS MC1000, MC1500, MC2000 is the device name listed in this FDA 510(k) record. The listed applicant is Meicor, Inc.. It received FDA 510(k) clearance on 1988-06-30 under 510(k) number K882323. The device is classified under product code ITY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

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

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