AC-POWERED MEDICAL EXAMINATION LIGHT— 510(k) K934259

Name: FDA 510(k) clearance K934259
Creator: U.S. Food and Drug Administration
Published: 1994-01-28

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K934259 for AC-POWERED MEDICAL EXAMINATION LIGHT, Substantially Equivalent on 1994-01-28. Applicant: Welch Allyn, Inc.. Device class: 1.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code KZF
Device class: Class 1
Regulation: 21 CFR 880.6320
Advisory panel: General Hospital
Date received: 1993-08-31
Decision date: 1994-01-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skaneateles Falls, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KZF

view all

K954943 — NEVOSCOPE1996-03-27
K952835 — WELCH ALLYN VIDEO EPISCOPE1995-09-22
K945507 — H 5100, H 5200, H 53001994-12-09
K941869 — SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEG1994-08-03
K936088 — WAVE FLUORESCENT MAGNIFIER1994-04-26

More clearances from Welch Allyn, Inc.

view all

K243598 — Welch Allyn Connex® 360 (Multiple)2025-07-13
K241411 — Welch Allyn Connex® Spot Monitor; 901058 Vital Signs Monitor Core (CSM)2024-12-20
K223381 — iExaminer System with Panoptic Plus2023-03-15
K212473 — Welch Allyn Connex Central Station2022-10-28
K191013 — Welch Allyn Diagnostic Cardiology Suite 2.X.X with Spirometry option2019-09-10

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