510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K821923Substantially Equivalent

Table, Operating, Field 6530-00-709-8175

Emerson-Sack-Warner Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K821923 is the FDA 510(k) clearance record for TABLE, OPERATING, FIELD 6530-00-709-8175, a class I device, cleared for Emerson-Sack-Warner Corp. on under FDA product code FWX (Table, Operating-Room, Mechanical). FDA records list 4 510(k) clearances for Emerson-Sack-Warner Corp., from to . As of , FDA records show no recalls naming K821923.

Clearance record

Decision date
Received
(14 days to decision)
Product code
FWX Table, Operating-Room, Mechanical
Regulation
21 CFR 878.4950
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Emerson-Sack-Warner Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FWX

Trailing 12 months

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

FDA records show no clearances under product code FWX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FWX, 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