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FDA 510(k)

PTW DOSIMETRY DIODE, T60008

K-Number: K010916 · 2001-06-20

ApplicantPtw-New York Corp.
Decision Date2001-06-20
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PTW DOSIMETRY DIODE, T60008 is the device name listed in this FDA 510(k) record. The listed applicant is Ptw-New York Corp.. It received FDA 510(k) clearance on 2001-06-20 under 510(k) number K010916. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PTW DOSIMETRY DIODE, T60008?

PTW DOSIMETRY DIODE, T60008 is a medical device that received FDA 510(k) clearance on 2001-06-20. The listed applicant is Ptw-New York Corp.. The 510(k) number is K010916.

When did PTW DOSIMETRY DIODE, T60008 receive FDA 510(k) clearance?

PTW DOSIMETRY DIODE, T60008 received FDA 510(k) clearance on 2001-06-20, under 510(k) number K010916.

Who is the listed applicant for PTW DOSIMETRY DIODE, T60008?

The FDA 510(k) record lists Ptw-New York Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PTW DOSIMETRY DIODE, T60008?

The FDA product code for PTW DOSIMETRY DIODE, T60008 is IYE.

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Other records listing Ptw-New York Corp. as applicant

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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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