Product code DPA— Clinical Chemistry

FDA has cleared 5 devices under product code DPA between 1976 and 1991, filed by 5 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.

• 19911 clearance
• 19891 clearance
• 19791 clearance
• 19771 clearance
• 19761 clearance

• Technicon Instruments Corp.1 clearance
• Gelman Sciences, Inc.1 clearance
• G.D. Searle and Co.1 clearance
• Dyna-Tek Industries1 clearance
• Ackerman Nuclear, Inc.1 clearance

• K904326 — DE-TOX TUBES A AND DE-TOX TUBES BDyna-Tek Industries·1991-01-17
• K884176 — CHROMATOGRAPHY KITGelman Sciences, Inc.·1989-04-04
• K791431 — TECHNICON FAST-LC SYS. FOR THEOPHYLLINETechnicon Instruments Corp.·1979-10-11
• K770765 — REAGENT SET, RENORPACEG.D. Searle and Co.·1977-06-24
• K760908 — MINIATURE ASCENDING PAPER CHROMATO-Ackerman Nuclear, Inc.·1976-11-19