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FDA 510(k)

MG-1001 TUBE HOUSING ASSEMBLY

K-Number: K921316 · 1992-06-22

ApplicantMagma Corp.
Decision Date1992-06-22
Product CodeITY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MG-1001 TUBE HOUSING ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Magma Corp.. It received FDA 510(k) clearance on 1992-06-22 under 510(k) number K921316. 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 MG-1001 TUBE HOUSING ASSEMBLY?

MG-1001 TUBE HOUSING ASSEMBLY is a medical device that received FDA 510(k) clearance on 1992-06-22. The listed applicant is Magma Corp.. The 510(k) number is K921316.

When did MG-1001 TUBE HOUSING ASSEMBLY receive FDA 510(k) clearance?

MG-1001 TUBE HOUSING ASSEMBLY received FDA 510(k) clearance on 1992-06-22, under 510(k) number K921316.

Who is the listed applicant for MG-1001 TUBE HOUSING ASSEMBLY?

The FDA 510(k) record lists Magma Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MG-1001 TUBE HOUSING ASSEMBLY?

The FDA product code for MG-1001 TUBE HOUSING ASSEMBLY 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.K923094MOLYBDENUMSoutheastern Medical Diagnostics, Inc.K923141PHILIPS PRE-FILTER OPTIONPhilips Medical Systems, Inc.K921129MRX-700Mrx-Ray Tube Corp.K921130MRX-865Mrx-Ray Tube Corp.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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