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Company · US

Micro Direct, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2004. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
BZG	Spirometer, Diagnostic	3
NRH	System, Breath Measurement	2
BZH	Meter, Peak Flow, Spirometry	1
CAH	Filter, Bacterial, Breathing-Circuit	1
CAP	Monitor, Airway Pressure (Includes Gauge And/Or Alarm)	1
CCJ	Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
May 19, 2004	K033688	MICRO H2 BREATH MONITORING DEVICE WITH HYDRA SOFTWARE UTILITY Micro Direct, Inc.	NRH
Dec 1, 2003	K031102	MICROLAB SPIROMETER Micro Direct, Inc.	BZG
Aug 27, 2003	K030586	MICROPEAK Micro Direct, Inc.	BZH
Nov 21, 1997	K973314	SPIROSAFE FILTER Micro Direct, Inc.	CAH
Jun 17, 1997	K965042	MICRODL DIARYCARD SPIROMETER Micro Direct, Inc.	BZG
Jan 24, 1997	K963376	MICRO H2 Micro Direct, Inc.	NRH
Nov 1, 1996	K963035	MICRO SPIROMETER Micro Direct, Inc.	BZG
Oct 17, 1996	K950197	MICROCO Micro Direct, Inc.	CCJ
Nov 21, 1994	K940375	MICRO MPM Micro Direct, Inc.	CAP

Latest recalls

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

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