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

VITALOGRAPH 2110 SOFTWARE INTERFACE

K Number: K950854 · Decision Oct 12, 1995
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
17
Review Days
227

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
VITALOGRAPH 2110 SOFTWARE INTERFACE
K Number
K950854
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vitalograph , Ltd.
Date Received
February 27, 1995
Decision Date
October 12, 1995
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

Similar 510(k) Clearances

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

View all

Other Clearances by Vitalograph , Ltd.

K Number Device Name
K253293 VitaloJAK Clinic (Model 7100)
K925085 ESCORT SPIROMETER
K930085 VITALOGRAPH DATA STORAGE SPIROMETER
K912412 VITALOGRAPH SPIROTRAC III
K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
Search all 17 clearances from Vitalograph , Ltd. →