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Ipax, Inc.

FDA 510(k) & PMA Approved Devices — 18 products

Total Devices18
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K200893 ProntoPump Sterile Tube SetLHI2021-05-04 View
510(k) K971242 BLINK GOLD EVELID WEIGHT (BG 06 THRU BG 28)MML1997-12-17 View
510(k) K971245 BLINK EXTERNAL EYELID WEIGHTMML1997-06-20 View
510(k) K915158 SUREBREATH DOME, E-Z BREATHERGAD1992-02-12 View
510(k) K915118 PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBEHQC1991-12-27 View
510(k) K914172 KPE 230 AMHQC1991-10-25 View
510(k) K914221 KPE 220 TS, NONSTERILEHQE1991-10-25 View
510(k) K884076 SUREBREATH DOMEGAD1988-10-07 View
510(k) K873097 PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKSGBQ1987-09-04 View
510(k) K870770 TIMLEINE(TM) VENIPUNCTURE SYSTEMKMK1987-04-23 View
510(k) K864726 I/A/KPE TIPHQC1987-01-20 View
510(k) K863729 OPHTHALMIC FITLER MICRO CAPSULEHQC1986-10-10 View
510(k) K863209 US PLUS-PAK(R) SURGICAL SYSTEMHQC1986-09-08 View
510(k) K862334 CATALOG NO. I/A 100 AND KPE 2001986-07-08 View
510(k) K861182 TIMELINE VENIPUNCTURE SYSTEMFPA1986-06-04 View
510(k) K860609 TIMELINE VENIPUNCTURE SYSTEMFPA1986-06-04 View
510(k) K833961 I/A PLUS PAK SURGICAL SYSTEMHQC1984-03-12 View
510(k) K833962 KPE PLUS-PAK SURGICAL SYSTEMHQC1984-03-12 View
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