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FDA 510(k)

PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY

K-Number: K021987 · 2002-12-27

Decision Date2002-12-27
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is S&S Par Scientific. It received FDA 510(k) clearance on 2002-12-27 under 510(k) number K021987. 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 PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY?

PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY is a medical device that received FDA 510(k) clearance on 2002-12-27. The listed applicant is S&S Par Scientific. The 510(k) number is K021987.

When did PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY receive FDA 510(k) clearance?

PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY received FDA 510(k) clearance on 2002-12-27, under 510(k) number K021987.

Who is the listed applicant for PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY?

The FDA 510(k) record lists S&S Par Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY?

The FDA product code for PARCOMPLAST COMPENSATING FILTER FOR RADIATION THERAPY 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.

Other records listing S&S Par Scientific 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.

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.

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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