510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K040772Substantially Equivalent

Pacific Recumbent Height-Adjustable Bath System

Penner Manufacturing, Inc., Ohaha NE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K040772 is the FDA 510(k) clearance record for PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEM, a class II device, cleared for Penner Manufacturing, Inc. on under FDA product code ILJ (Bath, Hydro-Massage). FDA records list 3 510(k) clearances for Penner Manufacturing, Inc., from to . As of , FDA records show 10 recalls naming K040772.

Clearance record

Decision date
Received
(10 days to decision)
Product code
ILJ Bath, Hydro-Massage
Regulation
21 CFR 890.5100
Device class
Class II
Review panel
Physical Medicine
Applicant
Penner Manufacturing, Inc. 1500 Woodmen Tower, Ohaha NE
510(k) summary
Statement
Third party review
Yes

Clearances, product code ILJ

Trailing 12 months

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

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