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

MODEL 8500 HAND HELD PULSE OXIMETER

K Number: K893221 · Decision Feb 28, 1990
Classifications
1
FEI Numbers
403
Registration Numbers
403
Same Product Code
711
Applicant Total
44
Review Days
307

Basic Information

Device Name
MODEL 8500 HAND HELD PULSE OXIMETER
K Number
K893221
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2700
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
NONIN MEDICAL, INC.
Date Received
April 27, 1989
Decision Date
February 28, 1990
Product Code
DQA
Advisory Committee
Cardiovascular
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
DQA Oximeter

Similar 510(k) Clearances

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

View all

Other Clearances by NONIN MEDICAL, INC.

K Number Device Name
K160231 Model X-100C CO-Met™ Oximetry System
K160865 Model 6100C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6100C Series: 6100CA, 6100CP, 6100CI, 6100CN), Model 6101C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6101C Series: 6101CA, 6101CP, 6101CI, 6101CN), Model 6102C Series Single-Patient Use, Disposable Pulse Oximeter Sensors (6102C Series: 6102CA, 6102CP, 6102CI, 6102CN), Model 8100AA/8100AP Reusable, Finger Clip Pulse Oximeter Sensor, Model 8101AA/8101AP Reusable, Finger Clip Pulse Oximeter Senso
K140785 PULSE OXIMETER
K132402 SENSMART MODEL X-100 UNIVERAL OXIMETRY SYSTEM
K131021 PULSE OXIMETER
K113215 MODEL 7600 REGIONAL OXIMETER SYSTEM WITH EQUANOX TECHNOLOGY
K112843 PULSE OXIMETER
K102350 PULSE OXIMETER
K102715 REGIONAL OXIMETER
K093853 SINGLE-PATIENT USE DISPOSABLE SENSOR SERIES
Search all 44 clearances from NONIN MEDICAL, INC. →