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FDA 510(k)

C.B. RADIOLOGY DESIGN GONADSHIELD

K-Number: K833523 · 1983-11-21

ApplicantRadiology Design
Decision Date1983-11-21
Product CodeIWT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

C.B. RADIOLOGY DESIGN GONADSHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Radiology Design. It received FDA 510(k) clearance on 1983-11-21 under 510(k) number K833523. The device is classified under product code IWT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.B. RADIOLOGY DESIGN GONADSHIELD?

C.B. RADIOLOGY DESIGN GONADSHIELD is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Radiology Design. The 510(k) number is K833523.

When did C.B. RADIOLOGY DESIGN GONADSHIELD receive FDA 510(k) clearance?

C.B. RADIOLOGY DESIGN GONADSHIELD received FDA 510(k) clearance on 1983-11-21, under 510(k) number K833523.

Who is the listed applicant for C.B. RADIOLOGY DESIGN GONADSHIELD?

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

What is the FDA product code for C.B. RADIOLOGY DESIGN GONADSHIELD?

The FDA product code for C.B. RADIOLOGY DESIGN GONADSHIELD is IWT.

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Related Devices (Code: IWT)

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.

K930763FIGLEAF SHIELDByers Industries, Inc.

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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