Atlas FDA

ANALYTIX AUTO SAMPLE PREP. STA. 1600

FDA 510(k) clearance K770210 · decided 1977-02-14

Clearance details

K-number
K770210
Device name
ANALYTIX AUTO SAMPLE PREP. STA. 1600
Applicant
G.D. Searle and Co.
Decision
Substantially Equivalent
Date received
1977-01-31
Decision date
1977-02-14
Days to decision
14 days
Clearance type
Traditional
Product code
JQW
Device class
1
Regulation number
862.2750
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
BD VIPER INSTRUMENT (K023955)Becton, Dickinson & CO2003-06-24
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2700 SAMPLE MANAGER (K980180)Waters Corporation1998-02-12
MASTERCAP AM 5.0/MASTERCAP RM 5.0 (K970420)Pharmacia, Inc.1997-06-30
MINI SAMPLER PROCESSOR (K970616)Cavro Scientific Instruments, Inc.1997-04-21
GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEM (K962687)Nichols Institute Diagnostics1997-03-28
MINI SAMPLE PROCESSOR (K962859)Cavro Scientific Instruments, Inc.1996-10-29
MICROLAB 4000, MICROLAB 4200 (K961896)Hamilton Co.1996-08-16
IMPACT (K961694)Matrix Technologies Corp.1996-06-21
GENESIS (K953345)Tecan U.S., Inc.1995-11-21
MEDTEC AUTOBLOT 2000 (K951753)Medtec, Inc.1995-10-17
ROBOCAP (K952025)Pharmacia, Inc.1995-07-26

Recalls involving this device

No recalls on record reference this clearance.