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

VAN DELLEN CANNULA

K Number: K873464 · Decision Nov 23, 1987
Classifications
1
FEI Numbers
331
Registration Numbers
331
Same Product Code
83
Applicant Total
7
Review Days
87

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
VAN DELLEN CANNULA
K Number
K873464
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Van Dellen, Ltd.
Date Received
August 28, 1987
Decision Date
November 23, 1987
Product Code
JOL
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
JOL Catheter And Tip, Suction

Similar 510(k) Clearances

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

View all

Other Clearances by Van Dellen, Ltd.

K Number Device Name
K873465 VAN DELLEN BACTERIA FILTER
K873463 VAN DELLEN ASPIRATING TUBING
K873462 VAN DELLEN ASPIRATOR
K873162 VAN DELLEN RETROBULBAR NEEDLE
K873163 VAN DELLEN IRRIGATING CYSTOTOME
K873164 VAN DELLEN HEALON CANNULA