BED SENTRY, MODEL 50U— 510(k) K850538

Substantially Equivalent

Metatech Corp.

FDA 510(k) clearance K850538 for BED SENTRY, MODEL 50U, Substantially Equivalent on 1985-04-03. Applicant: Metatech Corp.. Device class: 2.

Clearance details

Applicant: Metatech Corp.
Product code: Code KPN
Device class: Class 2
Regulation: 21 CFR 876.2040
Advisory panel: Gastroenterology, Urology
Date received: 1985-02-11
Decision date: 1985-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPN

K130951 — SIM2013-08-22
K971442 — HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-51998-01-08
K971855 — POTTY PAL AND FOREVER-DRY1997-08-18
K962770 — UROSURGE ACUTRAINER1996-08-01
K962416 — DRYTIME FOR BLADDER CONTROL SILENT1996-07-22

More clearances from Metatech Corp.

K924314 — MOBILE STANDING FRAME1993-02-12
K915370 — COPPER VAPOR LASER SYSTEM1992-02-07
K903883 — VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LES1990-09-19
K890865 — HEXASCAN SCANNER HANDPIECE1989-03-24
K883541 — METALASER VASCULASE1988-11-04

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