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

DOPCORD PPG

K Number: K884451 · Decision Jan 12, 1989
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
23
Review Days
80

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Basic Information

Device Name
DOPCORD PPG
K Number
K884451
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2780
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Huntleigh Technology, Inc.
Date Received
October 24, 1988
Decision Date
January 12, 1989
Product Code
JOM
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
JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic

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Other Clearances by Huntleigh Technology, Inc.

K Number Device Name
K992733 AKRON ATP9 TRACTION MACHINE
K964699 RHEO DOPPLEX II (RD 2)
K924516 OP3/VP4
K910188 FLOWPLUS AC330 PUMP GARMENTS
K900882 MULTI DOPPLEX, MD-1
K900618 HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140
K890012 HUNTLEIGH DYNAMIC FLOTATION SYSTEM
K881632 FLOWTRON DVT SYSTEM AC500 PUMP, L501 GARMENT
K874688 FLOWTRON AC200/2
K882644 HUNTLEIGH DOUBLE BUBBLE AIR-O-PAD-AOP5
Search all 23 clearances from Huntleigh Technology, Inc. →