Atlas FDA

AVI-D CONTROL

FDA 510(k) clearance K811713 · decided 1981-10-23

Clearance details

K-number
K811713
Device name
AVI-D CONTROL
Applicant
Ortho Diagnostic Systems, Inc.
Decision
Substantially Equivalent
Date received
1981-06-17
Decision date
1981-10-23
Days to decision
128 days
Clearance type
Traditional
Product code
KSF
Device class
2
Regulation number
864.9650
Medical specialty
Hematology
Advisory committee
Hematology
Location
Carpinteria, 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
DADE RH CONTROL REAGENT (K810599)American Dade1981-03-31
RH CONTROL (K801425)North American Biologicals, Inc.1980-07-14
RST-SERIES CONTROL (K800658)Gamma Biologicals, Inc.1980-04-16
ORTHO ANTISERA CONTROL (K800310)Ortho Diagnostics, Inc.1980-03-05
RH-HR NEGATIVE CONTROL REAGENT (K800239)Gotham Biologics, Inc.1980-02-21
TEST CELLS (K790249)Hyland Therapeutic Div., Travenol Laboratories1979-05-16
COUNTER CHECK, H001, H002, H003 (K790025)Diagnostic Technology, Inc.1979-01-17
RECAP (K780665)Bca Biological Corp. of America1978-06-06
QUALITY CONTROL SYSTEM, SPECTRA (K780097)Bd Becton Dickinson Vacutainer Systems Preanalytic1978-04-24
REAGENT CONFIDENCE SERA (K771814)Ortho Diagnostics, Inc.1977-11-07
UNIVAL CONTROL CELLS (K761284)Dade, Baxter Travenol Diagnostics, Inc.1977-01-25

Recalls involving this device

No recalls on record reference this clearance.