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FDA 510(k)

UNIVERSAL PATIENT CHAIR UNI 2000X

K-Number: K855063 · 1986-01-30

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1986-01-30
Product CodeJAI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL PATIENT CHAIR UNI 2000X is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K855063. The device is classified under product code JAI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL PATIENT CHAIR UNI 2000X?

UNIVERSAL PATIENT CHAIR UNI 2000X is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K855063.

When did UNIVERSAL PATIENT CHAIR UNI 2000X receive FDA 510(k) clearance?

UNIVERSAL PATIENT CHAIR UNI 2000X received FDA 510(k) clearance on 1986-01-30, under 510(k) number K855063.

Who is the listed applicant for UNIVERSAL PATIENT CHAIR UNI 2000X?

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

What is the FDA product code for UNIVERSAL PATIENT CHAIR UNI 2000X?

The FDA product code for UNIVERSAL PATIENT CHAIR UNI 2000X is JAI.

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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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