FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE

K Number: K113857 · Decision Apr 23, 2012
Classifications
1
FEI Numbers
26
Registration Numbers
27
Same Product Code
29
Applicant Total
16
Review Days
115

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SYNERGETICS DIRECTIONAL ENDOOCULAR LASER PROBE
K Number
K113857
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.4690
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synergetics, Inc.
Date Received
December 30, 2011
Decision Date
April 23, 2012
Product Code
HQB
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HQB Photocoagulator And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HQB), ordered by most recent decision date.

View all

Other Clearances by Synergetics, Inc.

K Number Device Name
K121426 AYNERGETICS DISPOSABLE SPETZLER-MALIS STANDARD BIPOLAR FORCEPS
K121675 VERSAVIT
K110924 DISPOSABLE SPETZLER-MALIS DUAL IRRIGATING BIPOLAR FORCEPS
K091441 SYNERGETICS ADJUSTABLE GAS PRESSURIZED INFUSION (AGPI) TUBE SET
K071482 STRYKER RF MULTI-LESION GENERATOR, MODEL 0406-900-000
K063489 STRYKER INTRADISCAL RF GENERATOR
K032598 SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE
K020220 ULTRASONIC STRAIGHT/ULTRASONIC KNIFE/ULTRASONIC RING CURRETTE
K010637 SONOTOME ULTRASONIC ASPIRATOR TIPS
K990568 SCRAMBLED ENDOOTO LASER PROBE, STRAIGHT TIP, MODEL 59.02, SCRAMBLED ENDOOTO LASER PROBE BENT TIP, MODEL 59.01
Search all 16 clearances from Synergetics, Inc. →