FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

SURGI SQUEEZ

K Number: K894927 · Decision Sep 11, 1989
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
34
Applicant Total
19
Review Days
40

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Basic Information

Device Name
SURGI SQUEEZ
K Number
K894927
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5420
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Ethox Corp.
Date Received
August 2, 1989
Decision Date
September 11, 1989
Product Code
KZD
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KZD Infusor, Pressure, For I.V. Bags

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
K935633 NO-MES
K921946 TUM-E-VAC BITE BLOCK
K885220 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
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
Search all 19 clearances from Ethox Corp. →