510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K870578Substantially Equivalent

Nightwatch(tm) System

Buckman Co., Inc., Martinez CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K870578 is the FDA 510(k) clearance record for NIGHTWATCH(TM) SYSTEM, a class II device, cleared for Buckman Co., Inc. on under FDA product code DSH (Recorder, Magnetic Tape, Medical). FDA records list 111 510(k) clearances for Buckman Co., Inc., from to . As of , FDA records show no recalls naming K870578.

Clearance record

Decision date
Received
(139 days to decision)
Product code
DSH Recorder, Magnetic Tape, Medical
Regulation
21 CFR 870.2800
Device class
Class II
Review panel
Cardiovascular
Applicant
Buckman Co., Inc. 921 Calle Verde, Martinez CA
Third party review
No

Clearances, product code DSH

Trailing 12 months
3 clearances under product code DSH in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DSH, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20261
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260