Atlas FDA

ENDOTRACHEAL TUBE CHANGERS

FDA premarket approval P800068/S002 · decided 1999-11-04

Approval details

PMA number
P800068
Supplement
S002
Supplement type
Normal 180 Day Track
Supplement reason
Express GMP Supplement
Trade name
ENDOTRACHEAL TUBE CHANGERS
Generic name
Changer, tube, endotracheal
Applicant
Instrumentation Industries, Inc.
Date received
1999-09-03
Decision date
1999-11-04
Days to decision
62 days
Decision code
APPR
Product code
LNZ
Advisory committee
Anesthesiology
Expedited review
No
Location
Pittsburg, PA
Statement
Approval for a manufacturing site located at FBK Medical Tubing, Inc., 511 Cobb St., Birmingham, AL 35209.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
NS 120P-TRS Airway Pressure Gauge (K180510)Instrumentation Industries, Inc.2019-05-01
RTC 26-C Inline Aerosol Adapter (K162753)Instrumentation Industries, Inc.2017-02-28
PILOT TUBE REPAIR KIT (K113644)Instrumentation Industries, Inc.2012-01-26
ENDOTRACHEAL TUBE CHANGERS (K102127)Instrumentation Industries, Inc.2010-08-27
RTC-24 VP METERED DOSE INHALER ADAPTER, MODEL RTC 24-V (K101857)Instrumentation Industries, Inc.2010-07-22
RTC METERED DOSE INHALER ADAPTERS-SINGLE PATIENT USE, MODEL RTC 24-V, RTC MDI ADAPTER KIT-SINGLE PATIENT USE, MODEL RTC (K091111)Instrumentation Industries, Inc.2009-12-02
NS SERIES VACUUM/PRESSURE GAUGES, CUFF PRESSURE MONITORS (K081778)Instrumentation Industries, Inc.2008-09-12
NS SERIES NIF (NEGATIVE INSPIRATORY FORCE) METERS (K081693)Instrumentation Industries, Inc.2008-09-11