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D.O.R.C. Disposable Cryo Probe

FDA 510(k) clearance K160591 · decided 2017-01-23

Clearance details

K-number
K160591
Device name
D.O.R.C. Disposable Cryo Probe
Applicant
Dutch Ophthalmic Research Center International BV
Decision
Substantially Equivalent
Date received
2016-03-01
Decision date
2017-01-23
Days to decision
328 days
Clearance type
Traditional
Product code
HRN
Device class
2
Regulation number
886.4170
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Zuidland, NL
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
MIRA Adapter (K200911)Phakos2020-06-02
Frigitronics adapter (K180195)Phakos2018-03-16
PHAKOS Disposable Retinal Cryo Probe (K162756)Phakos2017-05-03
CRYOMATIC MKII CONSOLE, CRYOMATIC MKII PROBES, DISPOSABLE CRYO PROBES (K131787)Keeler, Ltd.2013-12-23
CRYOMATIC CRYO CONSOLE, DISPOSABLE CRYO PROBE, DISPOSABLE PROBE ADAPTER (K112093)Keeler Instruments, Inc.2011-12-08
CRYOMATIC (K062412)Keeler Instruments, Inc.2006-11-06
D.O.R.C. CRYOSTAR CRYOSURGICAL SYSTEM (K012821)Dutch Ophthalmic USA, Inc.2001-10-22
KEELER CRYO MASTER & PROBES (K992954)Keeler Instruments, Inc.1999-12-21
CLIRANS TE08 HOLLOW FIBER DIALYZER (K823768)Terumo Medical Corp.1983-01-08

Recalls involving this device

No recalls on record reference this clearance.