510(k) K861162
- Device
- LENS SPECTACLE NON-CUSTOM (PRESCRIPTION)
- Applicant
- EFOP
- 510(k) number
- K861162
- Product code
- HQG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1986-06-09
- Date received
- 1986-03-28
- Regulation
- 886.5844
- Classification name
- Lens, Spectacle, Non-custom (prescription)
- Medical specialty
- Ophthalmic
- Review panel
- Ophthalmic
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- No
Applicant Contact#
- Contact
- CARREL.
- Address
- B P 193 13268 Marseille Cedex 8 France FR
FDA Registration Numbers#
- 3021376099
- 3030040625
- 9616258
- 3042284353
- 3010502837
- 3010613909
- 3030275066
- 3010183187
- 3011710819
- 3015242327
- 3004741385
- 3011644027
- 3031599350
- 3016671478
- 3013072273
- 9614727
- 3009494404
- 3017889035
- 3010625678
- 3010107381
- 3012409043
- 3014326379
- 3023876592
- 3007088216
- 3013151253
- 3012110814
- 8043609
- 8021087
- 8043304
- 8030290
- 3003372490
- 3034048670
- 3014931512
- 3017820141
- 3008396732
- 2083323
- 3005147601
- 3038285050
- 3003748653
- 3006748697
- 3010446957
- 3011589232
- 9616922
- 3012202690
- 3014518341
- 3015168505
- 3032027177
- 3006384133
- 3043126854
- 3030538356
- 3015169733
- 3033777988
- 8030300
- 3008044481
- 8020623
- 3020715708
- 3004110262
- 3037047283
- 3042285589
- 3026654653
- 3007113449
- 8020627
- 8022792
- 3016566587
- 3009490031
- 3003951061
- 3009405889
- 3022808
- 3013556952
- 3013603033
- 3014888885
- 9615499
- 3009005492
- 3011505252
- 3006356447
- 3013957868
- 3038136215
- 8043097
- 1293762
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HQG #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K935919 | SUNGLASSES | Ja-Ru, Inc. | 1994-02-16 |
| K920795 | 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX | Optical Radiation Corp. | 1992-07-13 |
| K900091 | MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR | Onufryk Low Vision Ent. | 1990-04-04 |
| K884360 | SEIKO P-6 PROGRESSIVE SPECTACLE LENSES | Seiko Corp. | 1988-11-15 |
| K882814 | NEOLENS PRESCRIPTION SPECTACLE LENS | Neolens, Inc. | 1988-07-29 |
| K882308 | CR-39 PLASTIC LENSES FOR EYEGLASSES | Automated Lens System | 1988-07-22 |
| K881225 | OPHTHALMIC SPECTACLE LENS BLANKS | Beta Optical Co, Inc. | 1988-04-19 |
| K875063 | SEIKO PLAX DIACOAT II & SEIKO PLAX S.V.P. | Epson EL Paso, Inc. | 1988-02-22 |
| K874681 | SWIRL - A PRE-MOISTENED CLEANING TISSUE FOR EYES | Klockner Contract Packaging, Inc. | 1988-02-05 |
| K873245 | AR DIACOAT SINGLE VISION LENSES | Seiko Optical Products of America, Inc. | 1987-10-05 |
| K872506 | MELANITE I | Aura Lens Products | 1987-07-27 |
| K871961 | MULTIPLE SPECTACLE LENS | Korea Asahi Optical Co., Ltd. | 1987-06-03 |
| K865103 | KROM-X LENS SYSTEM | Neo Optics, Inc. | 1987-01-20 |
| K863367 | FORMALENS 2000 | Vision-Sciences, Inc. | 1986-09-26 |
| K862578 | TECHNA VISION CASTING RESIN | Techna Vision | 1986-07-23 |
Legacy Summary#
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FDA Review#
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