FDA.reportPublic FDA data

PATHEN MEDICAL, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30148150983014815098PATHEN MEDICAL, LLC1Y2020-04-25271 Speciality Point Sanford FL US 32771

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
00850005864233PR-84214 - 14g x 1 1/4” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864240PR-84216 - 16g x 1 1/4” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864257PR-84218 - 18g x 1 1/4” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864264PR-84220 - 20g x 1 1/4” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864271PR-842202 - 20g x 1” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864288PR-84222 - 22g x 1” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864295PR-84224 - 24G x .75” IV CATHETER PURSAFETY R8773185421questions@pathen.com
00850005864301PS-84314 - 14g x 1.75” IV CATHETER PURSAFETY S8773185421questions@pathen.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2226361817806822K150513Imed Technology Intravascular Administration Set, Imed Technology Extension SetFPA2015-05-28

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FPA12015-05-28

GUDID#

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