BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK— 510(k) K932057

Name: FDA 510(k) clearance K932057
Creator: U.S. Food and Drug Administration
Published: 1994-08-05

Substantially Equivalent

Board of Directors, Albert Browne , Ltd.

FDA 510(k) clearance K932057 for BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK, Substantially Equivalent on 1994-08-05. Applicant: Board of Directors, Albert Browne , Ltd.. Device class: 2.

Clearance details

Applicant: Board of Directors, Albert Browne , Ltd.
Product code: Product code JOJ
Device class: Class 2
Regulation: 21 CFR 880.2800
Advisory panel: General Hospital
Date received: 1993-04-28
Decision date: 1994-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leics. Le4 Oaa, GB

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 Board of Directors, Albert Browne , Ltd.

view all

K971971 — BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK1998-07-10
K970918 — BROWNE STEAM INDICATOR1997-06-24
K922481 — BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE1994-06-02
K902958 — TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE1990-11-01

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