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

VACON TM

K Number: K770369 · Decision Mar 1, 1977
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
2
Applicant Total
12
Review Days
5

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
VACON TM
K Number
K770369
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Diemolding Corp.
Date Received
February 24, 1977
Decision Date
March 1, 1977
Product Code
CBD
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
CBD Bottle, Collection, Breathing System (Calibrated)

Similar 510(k) Clearances

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

View all

Other Clearances by Diemolding Corp.

K Number Device Name
K962749 THERAPEP W/MOUTHPIECE, W/PEDIATRIC MASK, W/SMALL MASK, W/LARGE MASK, RESISTOR/PORT/MOUTHPIECE, RESISTOR/PORT
K961455 MEDSHIELD/AEROCHAMBER
K902713 ACCESS. KIT FOR THE BIOSURGE SYNCHRONOUS AUTOTRANS
K902114 CUFF-MATE 2 ENDOTRACHEAL CUFF INFLATOR & MONITOR
K900754 RESPIREX 2
K893791 BREATHING MOUTHPIECE
K781759 RESCAL
K780750 O2 CONNECTOR
K760931 I.V. DRIP MONITOR ALARM DEVICE, MONIFLO
K760636 ORTHOMIX
Search all 12 clearances from Diemolding Corp. →