510(k) K843992
- Device
- CILCOR OPHTHALMIC INSTRUMENTS
- Applicant
- CILCO, INC.
- 510(k) number
- K843992
- Product code
- HNR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1984-11-21
- Date received
- 1984-10-11
- Regulation
- 886.4350
- Classification name
- Forceps, Ophthalmic
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- RICK MCCARLEY
- Address
- 1616 13th. Ave. Suite 200 Huntington WV US 25701 25701
FDA Registration Numbers#
- 2529392
- 8021817
- 3003039352
- 9613563
- 3003398873
- 2029275
- 3015451162
- 9614069
- 3003536766
- 9610612
- 3009465247
- 8043441
- 3010351679
- 9680563
- 3014334038
- 9615659
- 3006234743
- 8040381
- 3014257280
- 3015456951
- 8040884
- 9616250
- 3003365815
- 8010615
- 2431166
- 9614107
- 3005548740
- 3035451914
- 3005809810
- 9611516
- 3015972897
- 3036795921
- 3017970077
- 9680518
- 3015177648
- 8030973
- 3026790897
- 3030451558
- 8010374
- 3005067367
- 1932402
- 1421101
- 3015895045
- 8040449
- 3007589160
- 3042034415
- 3021680161
- 3004608878
- 1054241
- 1928237
- 1610287
- 8010733
- 9680260
- 3009703496
- 3004001706
- 1032347
- 3003759558
- 8010372
- 3029990829
- 9611502
- 9710524
- 3007583964
- 3012481881
- 3011371465
- 3008754084
- 1923569
- 8040179
- 3003972428
- 1058726
- 3008342610
- 3002675176
- 1039131
- 3010055973
- 9611112
- 3013421458
- 1929756
- 9610557
- 3017871343
- 9611503
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HNR #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K022835 | STEPHENS DISPOSABLE FORCEPS | Stephens Instruments | 2002-11-01 |
| K895434 | ALCON FOLDING FORCEPS | Alcon Laboratories | 1989-12-04 |
| K891487 | SOFT LENS FOLDING BLOCK | Western Medical Products, Inc. | 1989-08-15 |
| K893199 | PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTR | Allergan Medical Optics | 1989-06-16 |
| K885230 | MCDONALD FOLDING FORCEPS | Alcon Laboratories | 1989-05-17 |
| K881049 | BRADBURY INTRAOCULAR RETINAL KIT CAT #200 | Microline Pentax, Inc. | 1988-09-12 |
| K883197 | IOL IMPLANTATION FORCEPS | D & D Surgical | 1988-08-22 |
| K880274 | ADVANCED SURGICAL PRODUCTS SCLERAL PLUG FORCEPS | Advanced Surgical Products, Inc. | 1988-02-05 |
| K864266 | OPHTHALMIC KNIFE & FORCEPS | Western Medical Products, Inc. | 1986-11-28 |
| K864183 | OPHTHALMIC SURGICAL INSTRUMENTS | Techno Ophthalmics Intl. | 1986-11-28 |
| K864071 | FAULKNER FORCEPS | Staar Surgical Co. | 1986-11-13 |
| K863992 | THORNTON TITANIUM FORCEPS (VARIOUS TYPES) | Keeler Instruments, Inc. | 1986-10-31 |
| K863727 | FIXATION INSTRUMENTS | Medical Technology Development Corp. | 1986-10-31 |
| K863991 | THORTON TITANIUM NEEDLEHOLDERS(NO,W CATCH & STAND | Keeler Instruments, Inc. | 1986-10-31 |
| K864003 | PACO-FOLDER (TM) INTRAOCULAR LENS FORCEPS | Allergan, Inc. | 1986-10-31 |
Legacy Summary#
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FDA Review#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases