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FDA 510(k)

PHOENIX 60/60 PROCESSOR MODULE

K-Number: K831134 · 1983-11-07

ApplicantPhoenix Corp.
Decision Date1983-11-07
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PHOENIX 60/60 PROCESSOR MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Corp.. It received FDA 510(k) clearance on 1983-11-07 under 510(k) number K831134. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX 60/60 PROCESSOR MODULE?

PHOENIX 60/60 PROCESSOR MODULE is a medical device that received FDA 510(k) clearance on 1983-11-07. The listed applicant is Phoenix Corp.. The 510(k) number is K831134.

When did PHOENIX 60/60 PROCESSOR MODULE receive FDA 510(k) clearance?

PHOENIX 60/60 PROCESSOR MODULE received FDA 510(k) clearance on 1983-11-07, under 510(k) number K831134.

Who is the listed applicant for PHOENIX 60/60 PROCESSOR MODULE?

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

What is the FDA product code for PHOENIX 60/60 PROCESSOR MODULE?

The FDA product code for PHOENIX 60/60 PROCESSOR MODULE is DSF.

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Related Devices (Code: DSF)

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

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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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