510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K891023Substantially Equivalent

Siemens Ceiling Stand 800F, 800 and 810

Siemens Medical Electronics, Danvers MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891023 is the FDA 510(k) clearance record for SIEMENS CEILING STAND 800F, 800 AND 810, cleared for Siemens Medical Electronics on under FDA product code LDQ. FDA records list 15 510(k) clearances for Siemens Medical Electronics, from to . As of , FDA records show no recalls naming K891023.

Clearance record

Decision date
Received
(147 days to decision)
Product code
LDQ
Review panel
General Hospital
Applicant
Siemens Medical Electronics 16 Electronics Ave., Danvers MA
Third party review
No

Clearances, product code LDQ

Trailing 12 months

FDA records hold no clearances under product code LDQ in the trailing twelve months.

FDA records show no clearances under product code LDQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260