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FDA 510(k)

DUAL RADIATION TARGETING SYSTEM DRTS DRAPE

K-Number: K973162 · 1997-11-20

ApplicantHogan & Hartson
Decision Date1997-11-20
Product CodeIWE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DUAL RADIATION TARGETING SYSTEM DRTS DRAPE is the device name listed in this FDA 510(k) record. The listed applicant is Hogan & Hartson. It received FDA 510(k) clearance on 1997-11-20 under 510(k) number K973162. The device is classified under product code IWE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL RADIATION TARGETING SYSTEM DRTS DRAPE?

DUAL RADIATION TARGETING SYSTEM DRTS DRAPE is a medical device that received FDA 510(k) clearance on 1997-11-20. The listed applicant is Hogan & Hartson. The 510(k) number is K973162.

When did DUAL RADIATION TARGETING SYSTEM DRTS DRAPE receive FDA 510(k) clearance?

DUAL RADIATION TARGETING SYSTEM DRTS DRAPE received FDA 510(k) clearance on 1997-11-20, under 510(k) number K973162.

Who is the listed applicant for DUAL RADIATION TARGETING SYSTEM DRTS DRAPE?

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

What is the FDA product code for DUAL RADIATION TARGETING SYSTEM DRTS DRAPE?

The FDA product code for DUAL RADIATION TARGETING SYSTEM DRTS DRAPE is IWE.

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Other records listing Hogan & Hartson 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: IWE)

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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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