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FDA 510(k)

MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR

K-Number: K913577 · 1991-11-05

Decision Date1991-11-05
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Control-X, Inc.. It received FDA 510(k) clearance on 1991-11-05 under 510(k) number K913577. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR?

MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR is a medical device that received FDA 510(k) clearance on 1991-11-05. The listed applicant is Control-X, Inc.. The 510(k) number is K913577.

When did MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR receive FDA 510(k) clearance?

MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR received FDA 510(k) clearance on 1991-11-05, under 510(k) number K913577.

Who is the listed applicant for MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR?

The FDA 510(k) record lists Control-X, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR?

The FDA product code for MILESTONE MS 325 RADIOGRAPHIC X-RAY GENERATOR is IZO.

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.

Other records listing Control-X, 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.

View all 9 devices →

Related Devices (Code: IZO)

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

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