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FDA 510(k)

PANDOROS 1200A

K-Number: K811149 · 1981-06-09

ApplicantSiemens Corp.
Decision Date1981-06-09
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PANDOROS 1200A is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K811149. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANDOROS 1200A?

PANDOROS 1200A is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is Siemens Corp.. The 510(k) number is K811149.

When did PANDOROS 1200A receive FDA 510(k) clearance?

PANDOROS 1200A received FDA 510(k) clearance on 1981-06-09, under 510(k) number K811149.

Who is the listed applicant for PANDOROS 1200A?

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

What is the FDA product code for PANDOROS 1200A?

The FDA product code for PANDOROS 1200A is IZI.

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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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