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FDA 510(k)

THERATRON-PHOENIX

K-Number: K863180 · 1986-10-27

ApplicantAecl Medical
Decision Date1986-10-27
Product CodeIWB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THERATRON-PHOENIX is the device name listed in this FDA 510(k) record. The listed applicant is Aecl Medical. It received FDA 510(k) clearance on 1986-10-27 under 510(k) number K863180. The device is classified under product code IWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERATRON-PHOENIX?

THERATRON-PHOENIX is a medical device that received FDA 510(k) clearance on 1986-10-27. The listed applicant is Aecl Medical. The 510(k) number is K863180.

When did THERATRON-PHOENIX receive FDA 510(k) clearance?

THERATRON-PHOENIX received FDA 510(k) clearance on 1986-10-27, under 510(k) number K863180.

Who is the listed applicant for THERATRON-PHOENIX?

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

What is the FDA product code for THERATRON-PHOENIX?

The FDA product code for THERATRON-PHOENIX is IWB.

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Related Devices (Code: IWB)

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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