510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K032432Substantially Equivalent

Busse Hospital Disposables Spinal Manometer

Busse Hospital Disposables, Huntington CT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K032432 is the FDA 510(k) clearance record for BUSSE HOSPITAL DISPOSABLES SPINAL MANOMETER, a class II device, cleared for Busse Hospital Disposables, Inc. on under FDA product code FMJ (Manometer, Spinal-Fluid). FDA records list 35 510(k) clearances for Busse Hospital Disposables, Inc., from to . As of , FDA records show 7 recalls naming K032432.

Clearance record

Decision date
Received
(22 days to decision)
Product code
FMJ Manometer, Spinal-Fluid
Regulation
21 CFR 880.2500
Device class
Class II
Review panel
General Hospital
Applicant
Busse Hospital Disposables, Inc. P.O. Box 2156, Huntington CT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FMJ

Trailing 12 months

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

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