INTERP-1000— 510(k) K921476

Substantially Equivalent

Qmed, Inc.

FDA 510(k) clearance K921476 for INTERP-1000, Substantially Equivalent on 1992-10-21. Applicant: Qmed, Inc..

Clearance details

Applicant: Qmed, Inc.
Product code: Code LOS
Advisory panel: Unknown
Date received: 1992-03-30
Decision date: 1992-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Laurence Harbor, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LOS

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K023034 — CARDIOTOUCH-30002002-11-14
K011328 — CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPH2001-11-21

More clearances from Qmed, Inc.

K972991 — MONITOR ONE NDX1998-12-03
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K897121 — QEKG ELECTROCARDIOGRAPH1990-04-30
K873591 — A.R.M. (ASPEN RETURN MONITOR)1987-09-30
K862377 — QMED SELF ADHERING ELECTRODE1986-09-26

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