510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K952355Substantially Equivalent

The Hill Adjustable 90Md

Hill Laboratories, Malvern PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952355 is the FDA 510(k) clearance record for THE HILL ADJUSTABLE 90MD, a class I device, cleared for Hill Laboratories Co. on under FDA product code INQ (Table, Powered). FDA records list 17 510(k) clearances for Hill Laboratories Co., from to . As of , FDA records show no recalls naming K952355.

Clearance record

Decision date
Received
(56 days to decision)
Product code
INQ Table, Powered
Regulation
21 CFR 890.3760
Device class
Class I
Review panel
Physical Medicine
Applicant
Hill Laboratories Co. 445 Lincoln Hwy., Malvern PA
510(k) summary
Summary
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