Company · US

Brimfield Scientific Instruments

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1985. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
EQH	Source, Carrier, Fiberoptic Light	1
FCC	Endoscopic Magnetic Retriever	1
GDG	Hook, Surgical, General & Plastic Surgery	1
GDZ	Handle, Scalpel	1

Decided	510(k)	Device and applicant	Code
Jun 11, 1985	K852042	BRIMFIELD CANNULATED BLADE HOLDER Brimfield Scientific Instruments	GDZ
Sep 26, 1984	K843135	BRIMFIELD CANNULATED MAGNETIC RETRIEVER Brimfield Scientific Instruments	FCC
Sep 25, 1984	K843136	BRIMFIELD CANNULATED GRASPING HOOKS Brimfield Scientific Instruments	GDG
Jul 16, 1984	K841731	BRIMFIELD FIBEROPTIC LIGHT SCOURCE Brimfield Scientific Instruments	EQH
Jul 26, 1983	K832147	CIRCUT 1 Brimfield Scientific Instruments

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