510(k) K801467
- Device
- DODICK LENS HOLDING FORCEPS
- Applicant
- EDWARD WECK, INC.
- 510(k) number
- K801467
- Product code
- HNR
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1980-07-28
- Date received
- 1980-06-24
- 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#
- 8040233
- 9614069
- 3010407203
- 9680620
- 3027499529
- 3002675176
- 2084346
- 3003244954
- 8010518
- 1651405
- 9680718
- 3003398873
- 3015895045
- 9616250
- 8010099
- 3008902714
- 1836161
- 3004467263
- 3012375451
- 3003553186
- 3005225959
- 9611503
- 3035451914
- 3031231776
- 2521877
- 3005973280
- 1935627
- 3005548740
- 2031962
- 3016096142
- 3003803182
- 3009465247
- 1211998
- 1039131
- 3015177648
- 9615659
- 3014201171
- 3003759558
- 3039414397
- 8010257
- 1923569
- 3029082594
- 3006677911
- 8010510
- 3005440795
- 9611283
- 3006550126
- 3015456951
- 3032747418
- 1064371
- 3003365815
- 1720929
- 3021680161
- 8030973
- 3002692886
- 3005067367
- 3004215117
- 3012267976
- 3035642068
- 8010615
- 2531819
- 3010383847
- 3009027787
- 2529846
- 9611516
- 3017482348
- 3042228518
- 1421879
- 3002808022
- 3023657851
- 1226587
- 3002807115
- 2032098
- 3011110913
- 3004001706
- 3008828237
- 1032347
- 9615857
- 8010665
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#
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