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

BIOMEDIX PADNET LAB

K Number: K042616 · Decision Oct 12, 2004
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
11
Review Days
19

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Basic Information

Device Name
BIOMEDIX PADNET LAB
K Number
K042616
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2780
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomedix, Inc.
Date Received
September 23, 2004
Decision Date
October 12, 2004
Product Code
JOM
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

Similar 510(k) Clearances

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

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Other Clearances by Biomedix, Inc.

K Number Device Name
K142097 SELEC-3 I.V.ADMINISTRATION SET
K122281 PADNET 2.0
K073146 PADNET+
K050182 Q.STEPS BIOMETER G/C DUAL MONITORING SYSTEM
K033627 Q.STEPS BIOMETER G BLOOD GLUCOSE MONITORING SYSTEM
K973857 FLOSTAT VASCULAR REPORT GENERATOR (VRG)
K973644 FLOSTAT VASCULAR LAB
K961928 BIOMEDIX I.V. EXTENSION LINE W/ STOPCOCK MODEL B50-102/B51-102
K925645 SELEC-3
K926498 ENDOGRIP
Search all 11 clearances from Biomedix, Inc. →