FDA.reportPublic FDA data

ABLATIVE SOLUTIONS, INC.

Matched from indexed company URL: Ablative Solutions, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30103344443010334444ABLATIVE SOLUTIONS, INC.1N2026-01-01301 Edgewater Place Suite 100 Wakefield MA US 01880

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
00862468000318Peregrine System Infusion Catheter - Peregrine System Infusion Catheter, US650-688-9743producthandling@ablativesolutions.com
00862468000349Peregrine System™ Infusion Catheter - Peregrine System™ Infusion Catheter (4-7 mm), 510k, US650 688-9743info@ablativesolutions.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1596441702801740K231279Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmKRA2023-07-05
1596441420279253K140637PEREGRINE SYSTEM INFUSION CATHETERKRA2014-03-26
1596441935402555

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KRA22023-07-05

PMN#

GUDID#