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

CSPI SPECIMEN TRAP (NON-STERILE)

K Number: K870874 · Decision Apr 19, 1988
Classifications
1
FEI Numbers
193
Registration Numbers
193
Same Product Code
86
Applicant Total
4
Review Days
413

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
CSPI SPECIMEN TRAP (NON-STERILE)
K Number
K870874
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Custom Surgical Products, Inc.
Date Received
March 3, 1987
Decision Date
April 19, 1988
Product Code
GCX
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
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Similar 510(k) Clearances

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

View all

Other Clearances by Custom Surgical Products, Inc.

K Number Device Name
K841249 SUCTION CANNULAS
K841383 CSPI ROTARY SURGICAL ASPIRATOR
K841242 CSPI PREMIUM SURGICAL ASPIRATOR