Product code JTX— Microbiology

FDA has cleared 8 devices under product code JTX between 1976 and 1990, filed by 8 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 19902 clearances
• 19881 clearance
• 19791 clearance
• 19782 clearances
• 19762 clearances

• Scott Laboratories, Inc.1 clearance
• Medical Laboratory Automation Systems, Inc.1 clearance
• Marion Laboratories, Inc.1 clearance
• Gibco Laboratories Life Technologies, Inc.1 clearance
• Bd Becton Dickinson Vacutainer Systems Preanalytic1 clearance
• American Monitor Corp.1 clearance
• Acuson Corp.1 clearance
• Accu-Med Corp.1 clearance

• K901645 — ANAEROBIC ACCU-CULSHURE(TM)Medical Laboratory Automation Systems, Inc.·1990-07-16
• K897151 — ACUSON V328 AND C5432 TRANSDUCERSAcuson Corp.·1990-07-03
• K882637 — ACCU-CULSHURE TMAccu-Med Corp.·1988-07-06
• K791724 — BIO-BAG ENVIRONMENTAL CHAMBER (A & B)Marion Laboratories, Inc.·1979-10-17
• K781376 — STANDARDIZE TGCL & TGCHAmerican Monitor Corp.·1978-09-14
• K780159 — ANASWABScott Laboratories, Inc.·1978-02-13
• K761241 — PRE-DUCED SURGI-SWAB & TRANSPORTER TUBEGibco Laboratories Life Technologies, Inc.·1976-12-30
• K760063 — SPECIMEN COLLECTOR, ANAEROBICBd Becton Dickinson Vacutainer Systems Preanalytic·1976-08-03