510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220976Substantially Equivalent

Life Scope PT BSM-1700 Series Bedside Monitor

Nihon Kohden Corp., Tokyo, JP / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220976 is the FDA 510(k) clearance record for Life Scope PT BSM-1700 Series Bedside Monitor, a class II device, cleared for Nihon Kohden Corporation on under FDA product code KOI (Stimulator, Nerve, Peripheral, Electric). FDA records list 31 510(k) clearances for Nihon Kohden Corporation, from to . As of , FDA records show no recalls naming K220976.

Clearance record

Decision date
Received
(108 days to decision)
Product code
KOI Stimulator, Nerve, Peripheral, Electric
Regulation
21 CFR 868.2775
Device class
Class II
Review panel
Anesthesiology
Applicant
Nihon Kohden Corporation 1-31-4 Nishiochiai, Shinjuki-Ku, Tokyo, JP
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KOI

Trailing 12 months
1 clearance under product code KOI in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KOI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260