Ryder Contact Lens Case Model 10670
FDA 510(k) K951182 · Bradstreet Clinical Research Assoc., Inc.
510(k) numberK951182
Submission
- Device name
- Ryder Contact Lens Case Model 10670
- Applicant
- Bradstreet Clinical Research Assoc., Inc.
Brunswick, NJ, US - Received
- March 16, 1995
- Decision date
- May 16, 1995
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LRX – Case, Contact Lens
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 886.5928
- Specialty
- Ophthalmic
Other 510(k)s with product code LRX
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252175 | LANDR Contact LENS CaseLRX · Traditional | Fourth Axis, LLC | 02/10/2026SE |
| K250495 | Mini VP1 (PL67_F); Mini VP1 (PL61_F)LRX · Traditional | Avizor S.A. | 08/01/2025SE |
| K240095 | CAREUS Contact Lens Case (Model 1, Model 2, Model 3, Model 4, Model 5, Model 6)LRX · Traditional | Shanghai Care US Medical Product Co., Ltd. | 10/09/2024SE |
| K231123 | Phoenix Contact Lens Case - dome top flat pack (CL-01); Phoenix Contact Lens Case -…LRX · Traditional | Phoenix Innovative Healthcare Manufacturers Pvt.… | 08/30/2023SE |
| K173538 | Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODiscLRX · Special | Alcon Laboratories, Inc. | 12/04/2017SE |
| K172925 | Contact Lens Case, Model: A-1, B-1LRX · Traditional | P L Overseas Limited | 11/30/2017SE |
| K173365 | Bausch + Lomb Boston Scleral Lens CaseLRX · Traditional | Bausch & Lomb, Incorporated | 11/17/2017SE |
| K171539 | Contact Lens CaseLRX · Traditional | E-Link Plastic & Metal Industrial Co.,Ltd | 07/14/2017SE |
| K171163 | Contact Lens Case Round GlassesLRX · Traditional | Fiftytwoways, Ltd. | 06/27/2017SE |
| K162869 | Contact Lens CaseLRX · Traditional | Ningbo Yinzhou Zonghai Artware Co., Ltd. | 12/09/2016SE |
More from Ningbo Yinzhou Zonghai Artware Co., Ltd.
Questions and answers
When was Ryder Contact Lens Case Model 10670 cleared by the FDA?
Ryder Contact Lens Case Model 10670 (K951182) received a 510(k) decision of Substantially Equivalent on May 16, 1995, 61 days after the submission was received.
What is the product code of K951182?
The FDA product code is LRX – Case, Contact Lens, a Class II (moderate risk) device regulated under 21 CFR 886.5928.