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FDA 510(k)

DOSIMETRIC RELEASE OF RAD. TUBING PAC

K-Number: K833047 · 1985-06-11

ApplicantAmerican Bentley
Decision Date1985-06-11
Product CodeDWF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DOSIMETRIC RELEASE OF RAD. TUBING PAC is the device name listed in this FDA 510(k) record. The listed applicant is American Bentley. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K833047. The device is classified under product code DWF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOSIMETRIC RELEASE OF RAD. TUBING PAC?

DOSIMETRIC RELEASE OF RAD. TUBING PAC is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is American Bentley. The 510(k) number is K833047.

When did DOSIMETRIC RELEASE OF RAD. TUBING PAC receive FDA 510(k) clearance?

DOSIMETRIC RELEASE OF RAD. TUBING PAC received FDA 510(k) clearance on 1985-06-11, under 510(k) number K833047.

Who is the listed applicant for DOSIMETRIC RELEASE OF RAD. TUBING PAC?

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

What is the FDA product code for DOSIMETRIC RELEASE OF RAD. TUBING PAC?

The FDA product code for DOSIMETRIC RELEASE OF RAD. TUBING PAC is DWF.

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Related Devices (Code: DWF)

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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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