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FDA 510(k)

RSX 30HF

K-Number: K930792 · 1993-05-19

Decision Date1993-05-19
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RSX 30HF is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Imaging Corp.. It received FDA 510(k) clearance on 1993-05-19 under 510(k) number K930792. 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 RSX 30HF?

RSX 30HF is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Fischer Imaging Corp.. The 510(k) number is K930792.

When did RSX 30HF receive FDA 510(k) clearance?

RSX 30HF received FDA 510(k) clearance on 1993-05-19, under 510(k) number K930792.

Who is the listed applicant for RSX 30HF?

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

What is the FDA product code for RSX 30HF?

The FDA product code for RSX 30HF is IZO.

Other records listing Fischer Imaging Corp. 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 69 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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