SANISERV SURGICAL SLUSH SYSTEM— 510(k) K894006

Substantially Equivalent

Saniserv, Inc.

FDA 510(k) clearance K894006 for SANISERV SURGICAL SLUSH SYSTEM, Substantially Equivalent on 1989-11-03. Applicant: Saniserv, Inc.. Device class: 1.

Clearance details

Applicant: Saniserv, Inc.
Product code: Code JRM
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1989-06-05
Decision date: 1989-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JRM

K921568 — ORS-1001992-06-09
K921569 — ORS-2001992-06-09
K921570 — ORS-3001992-06-09
K915427 — ORS-10001992-01-07
K913777 — SELF-CONTAINED SURGICAL SLUSH FREEZER1991-09-25

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