510(k) K811658
- Device
- ANIS LENS IMPLANT FORCEPS #2
- Applicant
- AMERICAN V. MUELLER
- 510(k) number
- K811658
- Product code
- HNR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1981-06-26
- Date received
- 1981-06-12
- 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#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 1057946
- 8010518
- 3003553186
- 3010687973
- 3010041511
- 9611112
- 1651405
- 9616250
- 3007589160
- 3003644849
- 8040179
- 3003536766
- 3004475955
- 1036836
- 3013576617
- 9680718
- 3015451162
- 1720747
- 3036795921
- 1932402
- 3002807115
- 3031231776
- 9614062
- 3039414397
- 3029754081
- 3008797953
- 1032347
- 2246552
- 1928237
- 9680518
- 3017871343
- 3008828237
- 3029990829
- 3010155661
- 9612074
- 3002807310
- 3006234743
- 3015177648
- 3005595283
- 8010254
- 9613083
- 1421879
- 3003322138
- 3042228518
- 1646747
- 3004571672
- 3011110913
- 3030451558
- 9615745
- 3008102042
- 3014615697
- 3007589150
- 9610905
- 3002807090
- 3042940336
- 9710524
- 3005548740
- 3012267976
- 3012185136
- 3013938829
- 1412854
- 3007334784
- 3013466775
- 3021680161
- 3003418325
- 8010615
- 2084346
- 3003431869
- 3010383847
- 3015895045
- 2083373
- 2531819
- 8043816
- 3014257280
- 3042034415
- 3008808084
- 8010374
- 3007648354
- 1313525
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 |
| K864183 | OPHTHALMIC SURGICAL INSTRUMENTS | Techno Ophthalmics Intl. | 1986-11-28 |
| K864266 | OPHTHALMIC KNIFE & FORCEPS | Western Medical Products, Inc. | 1986-11-28 |
| K864071 | FAULKNER FORCEPS | Staar Surgical Co. | 1986-11-13 |
| K863727 | FIXATION INSTRUMENTS | Medical Technology Development Corp. | 1986-10-31 |
| K863991 | THORTON TITANIUM NEEDLEHOLDERS(NO,W CATCH & STAND | Keeler Instruments, Inc. | 1986-10-31 |
| K863992 | THORNTON TITANIUM FORCEPS (VARIOUS TYPES) | 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#
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