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FDA 510(k)

SIEMENS PHO/SONIC ALPHA 1000

K-Number: K802759 · 1981-01-07

ApplicantSiemens Gammasonics, Inc.
Decision Date1981-01-07
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS PHO/SONIC ALPHA 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K802759. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS PHO/SONIC ALPHA 1000?

SIEMENS PHO/SONIC ALPHA 1000 is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K802759.

When did SIEMENS PHO/SONIC ALPHA 1000 receive FDA 510(k) clearance?

SIEMENS PHO/SONIC ALPHA 1000 received FDA 510(k) clearance on 1981-01-07, under 510(k) number K802759.

Who is the listed applicant for SIEMENS PHO/SONIC ALPHA 1000?

The FDA 510(k) record lists Siemens Gammasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS PHO/SONIC ALPHA 1000?

The FDA product code for SIEMENS PHO/SONIC ALPHA 1000 is IYO.

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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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