Company · US

Keller Instruments, Inc.

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
HQA	Unit, Cryotherapy, Ophthalmic	2
GEN	Forceps, General & Plastic Surgery	1
HLJ	Ophthalmoscope, Battery-Powered	1
HLT	Preamplifier, Ac-Powered, Ophthalmic	1

Decided	510(k)	Device and applicant	Code
Dec 17, 1985	K854541	TIP OFF FORCEPS Keller Instruments, Inc.	GEN
Aug 15, 1984	K841294	ACU220 CRYO UNIT Keller Instruments, Inc.	HQA
May 9, 1984	K841293	PANORAMIC LOUPES - VARIOUS Keller Instruments, Inc.	HLT
May 9, 1984	K841292	SPECTACLE INDIRECT OPHTHALMOSCOPE Keller Instruments, Inc.	HLJ
Jan 17, 1983	K823835	SPEMBLY 140 CRYOSYSTEM PROBES & TIPS Keller Instruments, Inc.	HQA

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