OK Plus Indicator— 510(k) K222137

Name: FDA 510(k) clearance K222137
Creator: U.S. Food and Drug Administration
Published: 2022-12-05

Substantially Equivalent

Propper Manufacturing Co., Inc.

FDA 510(k) clearance K222137 for OK Plus Indicator, Substantially Equivalent on 2022-12-05. Applicant: Propper Manufacturing Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Manufacturing Co., Inc.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 2022-07-19
Decision date: 2022-12-05
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Long Island, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JOJ

view all

K263267 — Endox Test Strips2026-10-16
K261992 — 3M Attest Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)2026-09-25
K260181 — LF Process Indicator Tape for Steam Sterilization2026-02-20
K251991 — SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016) +1 more2025-12-23
K251035 — DISINTEK PA Test Strips2025-06-03

More clearances from Propper Manufacturing Co., Inc.

view all

K250306 — Chex-All Sterilization Pouches and Tubes2025-10-31
K240910 — EO Chex Indicator Tape2024-06-12
K212592 — Gas-Chex Indicator2022-01-20
K210866 — Steri-Dot Process Indicator2021-06-21
K210553 — Steam-Dot Process Indicator2021-05-19

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