FDA.reportPublic FDA data

CAMNTECH

Matched from indexed company URL: CAMNTECH LIMITED

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30074855973007485597CAMNTECH1N2026-01-01Manor Farm Fenstanton Cambridgeshire GB PE289JD
30088501823008850182CAMNTECH, INC.1Y2026-01-01630 Boerne Stage Airfield Boerne TX US 78006

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
B329AH420Actiheart - Ambulatory ECG recorder with acclerometer - single channel+1 830-755-8036sales@camntech.com
B329AWV01E22Actiwave - Ambulatory ECG/EEG recorder - single channel+1 830-755-8036sales@camntech.com
B329AWV02E25Actiwave - Ambulatory ECG/EEG recorder - two channel+1 830-755-8036sales@camntech.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
993151545622001K132764MOTION WATCH AND PRO-DIARYLEL2014-01-21
993151810059161K100266ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603MWJ2010-04-29
993151241350137K052489ACTIHEARTGWK2005-09-27

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LEL12014-01-21
MWJ12010-04-29
GWK12005-09-27

PMN#

GUDID#