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FDA 510(k)

SIEMENS CEILING STAND 800F, 800 AND 810

K-Number: K891023 · 1989-07-25

ApplicantSiemens Medical Electronics
Decision Date1989-07-25
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SIEMENS CEILING STAND 800F, 800 AND 810 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Electronics. It received FDA 510(k) clearance on 1989-07-25 under 510(k) number K891023. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS CEILING STAND 800F, 800 AND 810?

SIEMENS CEILING STAND 800F, 800 AND 810 is a medical device that received FDA 510(k) clearance on 1989-07-25. The listed applicant is Siemens Medical Electronics. The 510(k) number is K891023.

When did SIEMENS CEILING STAND 800F, 800 AND 810 receive FDA 510(k) clearance?

SIEMENS CEILING STAND 800F, 800 AND 810 received FDA 510(k) clearance on 1989-07-25, under 510(k) number K891023.

Who is the listed applicant for SIEMENS CEILING STAND 800F, 800 AND 810?

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

What is the FDA product code for SIEMENS CEILING STAND 800F, 800 AND 810?

The FDA product code for SIEMENS CEILING STAND 800F, 800 AND 810 is LDQ.

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Other records listing Siemens Medical Electronics as applicant

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Related Devices (Code: LDQ)

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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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