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

FILTERED VACUUM SAFETY TRAP BOTTLE

K Number: K855074 · Decision Mar 13, 1986
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
47
Applicant Total
38
Review Days
84

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
FILTERED VACUUM SAFETY TRAP BOTTLE
K Number
K855074
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Boehringer Laboratories
Date Received
December 19, 1985
Decision Date
March 13, 1986
Product Code
KDQ
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
KDQ Bottle, Collection, Vacuum

Similar 510(k) Clearances

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

View all

Other Clearances by Boehringer Laboratories

K Number Device Name
K234145 ViSiGi 3D Gastric Sizing Tube
K061788 BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM
K060277 BOEHRINGER LABORATORIES SUCTION PUMP SYSTEM
K020538 BOEHRINGER LABORATORIES PNEUMATIC AMBULATORY COMPRESSION SYSTEM 8200 SERIES
K014187 AUTOVAC ORTHOPEDIC AUTOTRANSFUSION SYSTEM
K013976 BOEHRINGER MRI SUCTION REGULATORY
K955010 AUTOVAC BP SYSTE, 2000 SERIES
K945775 BOEHRINGER AUTOVAC(R) 7900 SERIES
K932093 AUTOVAC CLOSED WOUND AUTOTRANSFUSION SYSTEM,7920 S
K933232 BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED
Search all 38 clearances from Boehringer Laboratories →