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SEDASYS COMPUTER-ASSISTED PERSONALIZED SEDATION SYSTEM

FDA premarket approval P080009 · decided 2013-05-03

Approval details

PMA number
P080009
Trade name
SEDASYS COMPUTER-ASSISTED PERSONALIZED SEDATION SYSTEM
Generic name
Computer-assisted personalized sedation system
Applicant
Scott Laboratories, Inc.
Date received
2008-03-25
Decision date
2013-05-03
Days to decision
1865 days
Decision code
APWD
Product code
PDR
Advisory committee
Anesthesiology
Expedited review
Yes
Location
Lubbock, TX
Statement
APPROVAL FOR THE SEDASYS® COMPUTER-ASSISTED PERSONALIZED SEDATION SYSTEM. THIS DEVICE IS INDICATED FOR THE INTRAVENOUS ADMINISTRATION OF 1% (10 MG/ML) PROPOFOL INJECTABLE EMULSION FOR THE INITIATION ANDMAINTENANCE OF MINIMAL TO MODERATE SEDATION, AS DEFINED BY THE AMERICAN SOCIETY OF ANESTHESIOLOGISTS (ASA) CONTINUUM OF DEPTH OF SEDATION, IN ASA PHYSICAL STATUS I AND II PATIENTS >= 18 YEARS OLD UNDERGOING COLONOSCOPY AND ESOPHAGOGASTRODUOD-DENOSCOPY (EGD) PROCEDURES.

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510(k) clearances by this applicant

RecordFirmDate
B. CAT CONFIRM (K880694)Scott Laboratories, Inc.1988-06-16
MUG-INDOLE DISC (K874933)Scott Laboratories, Inc.1988-01-05
MYCO-FLUOR REAGENT A & B (K874662)Scott Laboratories, Inc.1987-11-25
IDENTICULT-BL (K873509)Scott Laboratories, Inc.1987-10-15
ANABAG (K871238)Scott Laboratories, Inc.1987-04-03
SERO-STAT R II STAPHYLOCOCCUS TEST (K863025)Scott Laboratories, Inc.1986-09-15
SELECTICULT-CHLAMYDIA (K852869)Scott Laboratories, Inc.1985-09-19
IDENTICULT-NEISSERIA (K852832)Scott Laboratories, Inc.1985-07-19