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Company · US

Mcgaw Respiratory Therapy

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1977. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
CAF	Nebulizer (Direct Patient Interface)	4
BTR	Tube, Tracheal (W/Wo Connector)	1
CAI	Circuit, Breathing (W Connector, Adaptor, Y Piece)	1
CBD	Bottle, Collection, Breathing System (Calibrated)	1
CCI	Analyzer, Gas, Nitrogen, Gaseous-Phase	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Sep 20, 1977	K771550	MRT DISPENSOR Mcgaw Respiratory Therapy	CAF
Aug 16, 1977	K771516	CAPILLARY SAMPLE LINE Mcgaw Respiratory Therapy	CCI
Apr 15, 1977	K770665	VALVE, PRESSURE, DEMAND Mcgaw Respiratory Therapy	CBD
Feb 25, 1977	K770286	VENTILATOR BREATHING CIRCUIT Mcgaw Respiratory Therapy	CAI
Dec 30, 1976	K761300	NEBULIZER CONTROL UNIT Mcgaw Respiratory Therapy	CAF
Dec 30, 1976	K761299	DISPOSABLE NEBULIZER Mcgaw Respiratory Therapy	CAF
Dec 30, 1976	K761298	PRE-FILLED DISPOSABLE NEBULIZER Mcgaw Respiratory Therapy	CAF
Nov 19, 1976	K760998	ENDOTRACHAEL TUBE AND HOLDER Mcgaw Respiratory Therapy	BTR

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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