510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K925563Substantially Equivalent

Ft Model Table W/electric Hi Lo Option E

Pro Med Mfg., Inc., Blaine MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K925563 is the FDA 510(k) clearance record for FT MODEL TABLE W/ELECTRIC HI LO OPTION E, a class I device, cleared for Pro Med Mfg., Inc. on under FDA product code INQ (Table, Powered). FDA records list one 510(k) clearance for Pro Med Mfg., Inc. As of , FDA records show no recalls naming K925563.

Clearance record

Decision date
Received
(204 days to decision)
Product code
INQ Table, Powered
Regulation
21 CFR 890.3760
Device class
Class I
Review panel
Physical Medicine
Applicant
Pro Med Mfg., Inc. 10750 Mankato St., Blaine MN
510(k) summary
Statement
Third party review
No

Clearances, product code INQ

Trailing 12 months

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

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