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

SURGI-CUF STERILE/NON-STERILE DISPOSABLE

K Number: K883977 · Decision Feb 10, 1989
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
197
Applicant Total
19
Review Days
143

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Basic Information

Device Name
SURGI-CUF STERILE/NON-STERILE DISPOSABLE
K Number
K883977
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1120
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ethox Corp.
Date Received
September 20, 1988
Decision Date
February 10, 1989
Product Code
DXQ
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DXQ Blood Pressure Cuff

Similar 510(k) Clearances

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

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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
K935633 NO-MES
K921946 TUM-E-VAC BITE BLOCK
K885220 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
K894927 SURGI SQUEEZ
K860599 ETHOX LAVAGE TUBE
K844988 ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.
K841512 ETHOX RELIA-FLO 2001 ENTERAL FEED
Search all 19 clearances from Ethox Corp. →