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

BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)

K Number: K950897 · Decision Aug 24, 1995
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
112
Applicant Total
3
Review Days
178

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
BIOBOX TRAPTOP (SMALL, MEDIUM, LARGE AND X-LARGE)
K Number
K950897
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biosystems
Date Received
February 27, 1995
Decision Date
August 24, 1995
Product Code
MMK
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
MMK Container, Sharps

Similar 510(k) Clearances

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

View all

Other Clearances by Biosystems

K Number Device Name
K950898 BIOBOX WITH FUNNEL TOP (SMALL, MEDIUM, LARGE, AND X-LARGE)
K950899 LABORATORY SHARPS BARREL