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

VITALOGRAPH-EC60 HYDROGEN MONITOR

K Number: K874892 · Decision Jun 2, 1988
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
3
Applicant Total
17
Review Days
184

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-EC60 HYDROGEN MONITOR
K Number
K874892
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1820
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Vitalograph , Ltd.
Date Received
December 1, 1987
Decision Date
June 2, 1988
Product Code
NRH
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
NRH System, Breath Measurement

Similar 510(k) Clearances

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

View all

Other Clearances by Vitalograph , Ltd.

K Number Device Name
K253293 VitaloJAK Clinic (Model 7100)
K950854 VITALOGRAPH 2110 SOFTWARE INTERFACE
K925085 ESCORT SPIROMETER
K930085 VITALOGRAPH DATA STORAGE SPIROMETER
K912412 VITALOGRAPH SPIROTRAC III
K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
Search all 17 clearances from Vitalograph , Ltd. →