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FDA 510(k)

MOLYBDENUM

K-Number: K923094 · 1993-03-04

ApplicantSoutheastern Medical Diagnostics, Inc.
Decision Date1993-03-04
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MOLYBDENUM is the device name listed in this FDA 510(k) record. The listed applicant is Southeastern Medical Diagnostics, Inc.. It received FDA 510(k) clearance on 1993-03-04 under 510(k) number K923094. 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 MOLYBDENUM?

MOLYBDENUM is a medical device that received FDA 510(k) clearance on 1993-03-04. The listed applicant is Southeastern Medical Diagnostics, Inc.. The 510(k) number is K923094.

When did MOLYBDENUM receive FDA 510(k) clearance?

MOLYBDENUM received FDA 510(k) clearance on 1993-03-04, under 510(k) number K923094.

Who is the listed applicant for MOLYBDENUM?

The FDA 510(k) record lists Southeastern Medical Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOLYBDENUM?

The FDA product code for MOLYBDENUM is ITY.

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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.

K000052X-RAY MONOBLOCK, MONOBLOCK XRS-60-330Dynarad Corp.K933162MRX-750Mrx Corp.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.K921316MG-1001 TUBE HOUSING ASSEMBLYMagma Corp.

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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