3M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE— 510(k) K931605

Name: FDA 510(k) clearance K931605
Creator: U.S. Food and Drug Administration
Published: 1993-07-20

Substantially Equivalent

3M Health Care, Ltd.

FDA 510(k) clearance K931605 for 3M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE, Substantially Equivalent on 1993-07-20. Applicant: 3M Health Care, Ltd.. Device class: 1.

Clearance details

Applicant: 3M Health Care, Ltd.
Product code: Code IWZ
Device class: Class 1
Regulation: 21 CFR 892.1840
Advisory panel: Radiology
Date received: 1993-04-01
Decision date: 1993-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IWZ

view all

K970154 — KODAK EKTASIAN HG FILM (EHG-15)1997-04-04
K954200 — VOXGRAM1995-09-29
K931604 — 3M MEDICAL DIAGNOSTIC VIDEOCASSETTE1993-07-21
K920539 — ORWO X-RAY FILM1992-06-30
K884827 — KODAK DENTAL BARRIER PAC1989-01-30

More clearances from 3M Health Care, Ltd.

view all

K953904 — SARNS 9000 UNIVERSAL ROLLER PUMP1996-04-19
K926364 — ATTEST BRAND RAPID READOUT BIOLOGICAL IND. #129X1995-03-31
K941534 — MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEM1995-03-06
K941748 — STERI-VAC GAS STERILIZER MODEL 8XL1994-12-02
K930681 — 3M PREVENTION FABRIC SURGICAL GOWN #78XX1994-02-10

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