Matthew McClure FDA Filings

FDA Registration(s)#

Registration, FEI, Name table
Registration	FEI	Name	Status	Initial importer	Expiration year	Address
3007663004	3007663004	Matthew McClure	1	N	2026-01-01	137 Commercial St, #200 Plainview NY US 11803

Registration key, Listing key, Premarket submission table
Registration key	Listing key	Premarket submission	Device	Product code	Decision date
103411	1362947529	K111180	VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304, VASOMEDICAL-BIOX 3- CHANNEL MINIATURE AMBULATORY	DSH	2011-06-28
103411	1453441580	K111096	VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY	DSH	2011-06-24
103411	2034488228	K092785	COMBINED VASOMEDICAL-BIOX AMBULATORY ECG & BLOOD PRESSURE RECORDER & ANALYSIS SOFTWARE, 2301	DSH	2010-04-02
103411	1419054613	K083820	VASOMEDICAL BIOX CB-1305-C, 3 CHANNEL ECG HOLTER MONITOR, MODEL CB-1305-C	DSH	2009-04-01
103411	1234041169	K033617	EECP THERAPY SYSTEM MODEL TS4 WITH/WITHOUT PLUSE OXIMETRY	DRN	2004-03-01

Product code, Registration listing records, Latest decision table
Product code	Registration listing records	Latest decision
DSH	4	2011-06-28
DRN	1	2004-03-01