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FDA 510(k)

PCX 650HF RADIOGRAPHIC X-RAY

K-Number: K920351 · 1993-02-12

Decision Date1993-02-12
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PCX 650HF RADIOGRAPHIC X-RAY 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 1993-02-12 under 510(k) number K920351. 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 PCX 650HF RADIOGRAPHIC X-RAY?

PCX 650HF RADIOGRAPHIC X-RAY is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Control-X, Inc.. The 510(k) number is K920351.

When did PCX 650HF RADIOGRAPHIC X-RAY receive FDA 510(k) clearance?

PCX 650HF RADIOGRAPHIC X-RAY received FDA 510(k) clearance on 1993-02-12, under 510(k) number K920351.

Who is the listed applicant for PCX 650HF RADIOGRAPHIC X-RAY?

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 PCX 650HF RADIOGRAPHIC X-RAY?

The FDA product code for PCX 650HF RADIOGRAPHIC X-RAY 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

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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