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Company · US

Brattle Instrument Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1981. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
HGM	System, Monitoring, Perinatal	3
HGI	Electrocautery, Gynecologic (And Accessories)	1
IXO	Synchronizer, Ecg / Respirator, Radiographic	1
IXQ	Table, Radiographic, Stationary Top	1
KLK	Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Apr 10, 1981	K810588	SYNCHRONIZER #208 Brattle Instrument Corp.	IXO
Feb 2, 1981	K802978	TRANSCUTANEOUS BLOOD OXYGEN MONITOR #300 Brattle Instrument Corp.	KLK
Oct 17, 1978	K781681	PHIPIOLOGICAL SYNCHRONIZER PART#205 Brattle Instrument Corp.	IXQ
Apr 26, 1977	K770692	MONITOR, FETAL, NO. L04-1100 Brattle Instrument Corp.	HGM
Mar 9, 1977	K770297	FETAL MONITOR, PART #100-11009 Brattle Instrument Corp.	HGM
Mar 9, 1977	K770296	FETAL MONITOR, PART #101-11009 Brattle Instrument Corp.	HGM
Mar 9, 1977	K770295	ABDOMINAL ECG PROCESSOR FOR FETAL MONI. Brattle Instrument Corp.	HGI

Latest recalls

Date	Firm and product	Code	Linked 510(k)
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