Atlas FDA

VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM

FDA 510(k) clearance K851945 · decided 1985-05-24

Clearance details

K-number
K851945
Device name
VARIAN AASP AUTOMATED SAMPLE PREP. SYSTEM
Applicant
Varian Assoc., Inc.
Decision
Substantially Equivalent
Date received
1985-05-03
Decision date
1985-05-24
Days to decision
21 days
Clearance type
Traditional
Product code
KZR
Device class
1
Regulation number
862.2260
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Palo Alto, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
2487 DUAL WAVELENGTH ABSORBANCE DETECTOR (K973074)Waters Corporation1997-10-06
USDT FLOW IMMUNOASSAY SYSTEM, MODEL 9000 (K931227)U.S. Drug Testing, Inc.1993-05-06
COLUMNS LIQUID CHROMATOGRAPHY DPM (K905538)Millpore Corp.1991-01-25
SYVA SOLID PHASE COLUMNS SYSTEM II (K861392)Syva Co.1986-06-13
SERIES 410 LC PUMP (K860197)The Perkin-Elmer Corp.1986-03-17
LIQUID CHROMATOGRAPH 400 (K843568)The Perkin-Elmer Corp.1984-11-20
VARIAN 2000 LIQUID CHROMATOGRAPHY ANALY (K841890)Varian Assoc., Inc.1984-06-14
LIQUID CHROMATOGRAPHIC DETECTOR LC-95 (K840977)The Perkin-Elmer Corp.1984-04-19
CHROM-PREP (K832201)Hamilton Co.1983-08-16
VISTA 54 LIQUID CHROMATOGRAPHY ANAL. SYS (K802725)Varian Assoc., Inc.1980-12-11
LIQUID CHROMATOGRAPH MODEL 850 (K780944)E.I. Dupont DE Nemours & Co., Inc.1978-07-27
LIQUID CHROMATOGRAPH MODEL 860 (K780945)E.I. Dupont DE Nemours & Co., Inc.1978-07-27

Recalls involving this device

No recalls on record reference this clearance.