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FDA 510(k)

DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST

K-Number: K883317 · 1989-04-26

ApplicantS & S X-Ray Products, Inc.
Decision Date1989-04-26
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST is the device name listed in this FDA 510(k) record. The listed applicant is S & S X-Ray Products, Inc.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K883317. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST?

DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is S & S X-Ray Products, Inc.. The 510(k) number is K883317.

When did DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST receive FDA 510(k) clearance?

DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST received FDA 510(k) clearance on 1989-04-26, under 510(k) number K883317.

Who is the listed applicant for DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST?

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

What is the FDA product code for DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST?

The FDA product code for DCD-1 (DIGITAL CONTOUR DETECT-RADIAT THERAPY) SYST is IXI.

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.

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Other records listing S & S X-Ray Products, 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.

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Related Devices (Code: IXI)

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.

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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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