CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695— 510(k) K870278

Name: FDA 510(k) clearance K870278
Creator: U.S. Food and Drug Administration
Published: 1987-02-20

Substantially Equivalent

Ryder Intl. Corp.

FDA 510(k) clearance K870278 for CONTACT LENS CASE W/POSTIVE HEAT INDI. MOD. #695, Substantially Equivalent on 1987-02-20. Applicant: Ryder Intl. Corp.. Device class: 2.

Clearance details

Applicant: Ryder Intl. Corp.
Product code: Code LPN
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 1987-01-27
Decision date: 1987-02-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arab, AL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LPN

view all

K253795 — MeniSept 3% Hydrogen Peroxide Cleaning & Disinfecting Solution2026-08-13
K222541 — Bausch + Lomb Preservative Free Lubricating and Rewetting Drops2022-12-06
K221263 — Aqua Naina Plus Sterile Saline Solution2022-10-12
K202932 — ABT12 multi-purpose solution2021-05-28
K210051 — OTE MPS 045 Multi-purpose Lens Care Solution2021-05-26

More clearances from Ryder Intl. Corp.

view all

K962611 — BARD EAGLE INFLATION DEVICE1996-10-21
K962151 — RYDER LACRIMAL INTUBATIONSET1996-09-18
K953522 — USCI IDEAL PTCA KIT1996-04-17
K920064 — OPTI-LENS CONTACT LENS CASE1992-03-04
K915082 — OPTI-LENS(TM) CONTACT LENS CASE1992-01-13

Adverse events under product code LPN

product code LPN

Injury: 333
Other: 8
Total: 341

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.