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
228
Registration Numbers
229
Same Product Code
648
Applicant Total
13
Review Days
183

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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.

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Other Clearances by Neomed, Inc.

K Number Device Name
K183540 Oral/Enteral Syringes with ENFit connector (12 mL to 60 mL), Low Dose Tip Oral/Enteral Syringes with ENFit connector (1 mL to 6 mL)
K161039 NeoConnect Oral/Enteral Syringes with ENFit connector (12 mL to 100 mL) and NeoConnect Low Dose Tip Oral/Enteral Syringes with ENFit connector (0.5 mL to 6mL)
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
Search all 13 clearances from Neomed, Inc. →