Atlas FDA

BN PROSPEC SYSTEM

FDA 510(k) clearance K001647 · decided 2000-09-26

Clearance details

K-number
K001647
Device name
BN PROSPEC SYSTEM
Applicant
Dade Behring, Inc.
Decision
Substantially Equivalent
Date received
2000-05-30
Decision date
2000-09-26
Days to decision
119 days
Clearance type
Traditional
Product code
JZW
Device class
1
Regulation number
866.4540
Medical specialty
Immunology
Advisory committee
Immunology
Location
P.O. Box 6101, Newark, DE, 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
BEHRING LASER NEPHELOMETER (K761234)Behring Diagnostics, Inc.1990-06-07
BEHRING NEPHELOMETER 100 (K892223)Behring Diagnostics, Inc.1989-05-04
TURBOX (K873401)Unipath , Ltd.1987-09-23
RRT SYSTEM LASER REFLECTOMETER ANALYZER (K873407)Incstar Corp.1987-09-23
BCM-302 COLLIMATING CONE & COMPENSATIN (K801949)B C Medical , Ltd.1980-10-03
DISC 120 TRANSPORTER (K801391)Travenol Laboratories, S.A.1980-07-14
LANCER L-INA BUFFER, POLYMER, WASH SOLU (K792014)Sherwood Medical Industries1979-11-13
IMMUNOCHEMISTRY SYS. MANUAL MODE (K781006)Beckman Instruments, Inc.1978-08-31
LASER STANDARD SERUM (K761235)Behring Diagnostics, Inc.1976-12-30
ANTISERUM HUMAN (PRO.) NEPHELOMETRIC GR. (K761236)Behring Diagnostics, Inc.1976-12-30

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
COBAS INTEGRA 400 PLUS CYCLOSPORINE (P920031/S003)Dade Behring, Inc.2002-07-24
COBAS INTEGRA CYCLOSPORINE (P920031/S002)Dade Behring, Inc.2002-02-26
EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY (P920031/S001)Dade Behring, Inc.2000-08-11
EMIT 2000 CYCLOSPORINE SPECIFIC ASSAY (P920031)Dade Behring, Inc.1996-10-02