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Company · US

Medac, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 1988. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
DRO	Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)	8
DRT	Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)	1
LDD	Dc-Defibrillator, Low-Energy, (Including Paddles)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Mar 7, 1988	K874319	MONITOR, ELECTROGRAPHIC Medac, Inc.	DRT
Jan 27, 1988	K874447	DISPOSABLE GEL DEFIBRILLATION/EXTERNAL PACING ELEC Medac, Inc.	DRO
Dec 15, 1987	K874090	300M ECG MONITRO/TRANSCUTANEOUS PACEMAKER Medac, Inc.	DRO
Nov 23, 1987	K874091	360D DC DEFIBRILLATOR Medac, Inc.	LDD
Apr 23, 1987	K871176	PACE 10 NON-INVASIVE EXTERNAL PACEMAKER Medac, Inc.	DRO
Mar 10, 1987	K864985	DISPOS GEL EXTERNAL PACING ELECTRODE/LOW IMPEDANCE Medac, Inc.	DRO
Mar 3, 1987	K864989	ETP 180A NON-INVASIVE EXTERNAL PACEMAKER Medac, Inc.	DRO
Mar 3, 1987	K864988	ETP 180E NON-INVASIVE EXTERNAL PACEMAKER Medac, Inc.	DRO
Mar 3, 1987	K864987	DISPOS GEL EXTERNAL PACING ELECTRODE/HI IMPEDANCE Medac, Inc.	DRO
Mar 3, 1987	K864986	ETP 300 NON-INVASIVE EXTERNAL PACEMAKER Medac, Inc.	DRO

Latest recalls

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

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