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FDA 510(k)

MDT UROLOGY TABLE

K-Number: K942485 · 1994-08-26

ApplicantMdt Corp., Inc.
Decision Date1994-08-26
Product CodeMMZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MDT UROLOGY TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Mdt Corp., Inc.. It received FDA 510(k) clearance on 1994-08-26 under 510(k) number K942485. The device is classified under product code MMZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MDT UROLOGY TABLE?

MDT UROLOGY TABLE is a medical device that received FDA 510(k) clearance on 1994-08-26. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K942485.

When did MDT UROLOGY TABLE receive FDA 510(k) clearance?

MDT UROLOGY TABLE received FDA 510(k) clearance on 1994-08-26, under 510(k) number K942485.

Who is the listed applicant for MDT UROLOGY TABLE?

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 UROLOGY TABLE?

The FDA product code for MDT UROLOGY TABLE is MMZ.

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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.

K960777MDT UNISPORE AND SPOR-TEST BIOLOGICALINDICATORK942486IMAGE FULL POWER EXAMINATION/MINOR SURGERY TABLEK924380MDT/HARVEY MODEL 7000 & 8000 CHEMICLAVEK926081DENTAL LIGHTK924955MDT/HARVEY MC-8 AND MC-10K932094BOVIE ULTRASONIC SURGICAL ASPIRATOR

View all 22 devices →

Related Devices (Code: MMZ)

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.

K033335LITHOSTAR MODULARIS WITH SHOCKWAVE SYSTEM CPLUSSiemens Medical Solutions USA, Inc.K954278BETA MULTI-PROCEDURE MOBILE UROLOGICAL TABLE, MODEL S5005Beta Medical Products, Inc.K942445SYNERGY IISynectics Medical, Inc.

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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