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

MINI PECG-MODIFICATION

K Number: K841148 · Decision Apr 17, 1984
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
21
Review Days
27

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Basic Information

Device Name
MINI PECG-MODIFICATION
K Number
K841148
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intersect Systems, Inc.
Date Received
March 21, 1984
Decision Date
April 17, 1984
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Intersect Systems, Inc.

K Number Device Name
K021636 ALBUMIN REAGENT
K011972 DIRECT BILIRUBIN REAGENT
K011692 HOMOGENEOUS ENZYMIC HOMOCYSTEINE REAGENT
K003892 TOTAL BILIRUBIN REAGENT
K983937 DUAL VIAL CREATININE REAGENT
K974833 CK-NAC REAGENT
K941807 INTERSECT SYSTEMS' NON-MERCURIC CHLORIDE REAGENT
K932888 INTERSECT SYSTEMS DIRECT AMYLASE REAGENT
K934039 INTERSECT SYSTEMS HDL CHOLESTEROL REAGENT SET
K932267 ENZYMATIC CO2 REAGENT, MODIFICATION
Search all 21 clearances from Intersect Systems, Inc. →