Atlas FDA

MINI BALLOON

FDA premarket approval P780011/S011 · decided 1988-10-18

Approval details

PMA number
P780011
Supplement
S011
Supplement type
Normal 180 Day Track
Supplement reason
Other
Trade name
MINI BALLOON
Generic name
Device, Vascular, for Promoting Embolization
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic
Date received
1988-05-31
Decision date
1988-10-18
Days to decision
140 days
Decision code
APPR
Product code
KRD
Advisory committee
Cardiovascular
Expedited review
No
Location
Franklin Lake, NJ

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510(k) clearances by this applicant

RecordFirmDate
BACTEC MGIT 960 SIR KITS (K003062)Bd Becton Dickinson Vacutainer Systems Preanalytic2001-06-06
0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE (K003553)Bd Becton Dickinson Vacutainer Systems Preanalytic2001-03-21
BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE (K003461)Bd Becton Dickinson Vacutainer Systems Preanalytic2001-02-01
B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/16 (K002938)Bd Becton Dickinson Vacutainer Systems Preanalytic2000-11-29
BD DIRECTIGEN FLU A+B (K001364)Bd Becton Dickinson Vacutainer Systems Preanalytic2000-06-28
MOXIFLOXACIN, 5 UG, BBL SENSI-DISC (K000762)Bd Becton Dickinson Vacutainer Systems Preanalytic2000-04-25
GATIFLOXACIN, 5 UG, BBL SENSI-DISC (K000829)Bd Becton Dickinson Vacutainer Systems Preanalytic2000-04-13
SYNERCID, 15 UG, BBL SENSI-DISC (K993186)Bd Becton Dickinson Vacutainer Systems Preanalytic1999-11-03