ANALYTIX AUTO SAMPLE PREP. STA. 1600— 510(k) K770210

Name: FDA 510(k) clearance K770210
Creator: U.S. Food and Drug Administration
Published: 1977-02-14

Substantially Equivalent

G.D. Searle and Co.

FDA 510(k) clearance K770210 for ANALYTIX AUTO SAMPLE PREP. STA. 1600, Substantially Equivalent on 1977-02-14. Applicant: G.D. Searle and Co.. Device class: 1.

Clearance details

Applicant: G.D. Searle and Co.
Product code: Code JQW
Device class: Class 1
Regulation: 21 CFR 862.2750
Advisory panel: Clinical Chemistry
Date received: 1977-01-31
Decision date: 1977-02-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JQW

view all

K023955 — BD VIPER INSTRUMENT2003-06-24
K973335 — QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)1998-04-30
K980180 — 2700 SAMPLE MANAGER1998-02-12
K970420 — MASTERCAP AM 5.0/MASTERCAP RM 5.01997-06-30
K970616 — MINI SAMPLER PROCESSOR1997-04-21

More clearances from G.D. Searle and Co.

view all

K821159 — IN-LINE OXYGEN MONITORING SYSTEM1982-05-25
K811068 — BYPASS COIL1981-05-27
K811071 — VENOUS OXYGEN PROBE1981-05-05
K803238 — INTRAVASCULAR CATHETER1981-04-23
K810630 — SILICONE ELASTOMER COATED LATEX FOLEY1981-03-31

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