FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

NEOMED ENTERAL ONLY EXTENSION SET

K Number: K100288 · Decision Aug 3, 2010
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
11
Review Days
183

Basic Information

Device Name
NEOMED ENTERAL ONLY EXTENSION SET
K Number
K100288
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NEOMED, INC.
Date Received
February 1, 2010
Decision Date
August 3, 2010
Product Code
KNT
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KNT Tubes, Gastrointestinal (And Accessories)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNT), ordered by most recent decision date.

View all

Other Clearances by NEOMED, INC.

K Number Device Name
K152857 NeoMed NeoConnect Enteral Syringes with ENFit Connector and compatible NeoSecure Tip Caps
K143344 NeoMed NeoConnect Enteral Syringes with ENFit Connector
K122373 NEOMED ORAL/ENTERAL SYRINGE
K120182 NEOMED GASTROINTESTINAL TUBE AND ACCESSORIES
K092908 NEOMED STERILE SYRINGE, MODELS SD-S1EO, SD-S3EO, SD-S630, SD-S12EO, SD-S20EO, SD-S35EO, SD-S60EO
K082238 NEOMED POLYURETHANE FEEDING TUBE
K081515 NEOMED DUAL LUMEN UMBILICAL CATHETER, MODELS S2UVC4.0, S2UVC5.0
K073596 NEOMED SINGLE LUMEN UMBILICAL CATHETER
K072881 NEOMED Enteral FEEDING TUBE
K072997 NEOMED URINARY CATHETER
Search all 11 clearances from NEOMED, INC. →