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

NO-MES

K Number: K935633 · Decision Sep 30, 1994
Classifications
1
FEI Numbers
242
Registration Numbers
243
Same Product Code
648
Applicant Total
19
Review Days
311

Basic Information

Device Name
NO-MES
K Number
K935633
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5980
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ETHOX CORP.
Date Received
November 23, 1993
Decision Date
September 30, 1994
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

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Other Clearances by ETHOX CORP.

K Number Device Name
K040286 ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS
K031195 CUF-COVER (TM)
K962850 TUM-E-VAC
K921946 TUM-E-VAC BITE BLOCK
K885220 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
K894927 SURGI SQUEEZ
K883977 SURGI-CUF STERILE/NON-STERILE DISPOSABLE
K860599 ETHOX LAVAGE TUBE
K844988 ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.
K841512 ETHOX RELIA-FLO 2001 ENTERAL FEED
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