Spectramed, Inc.
Spectramed, Inc. holds FDA 510(k) medical device clearances, first cleared 1987, most recent 1990.
Top product codes for Spectramed, Inc.
Recent clearances by Spectramed, Inc.
- K896122 — AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED
- K892941 — CCO SYSTEM MODEL SP1467,SP5567,SP6267
- K895323 — MODEL DT-BAL, BALANCE SAVER
- K894362 — MODEL DT-IUPC2 TRANSDUCER TIPPED DUAL LUMEN IUP
- K881857 — AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU.
- K885235 — SAFE-DRAW(TM) BLOOD SAMPLING RESERVOIR & ACCESS.
- K881825 — MODELS SP5825/SP5835/SP5845/SP5855 PERCU. SHEATH
- K875337 — HEPARIN COATED LUMINAL PACING CATHETER
- K880740 — MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE
- K873168 — SPECTRAMED DISPOSABLE TRANSDUCER (DT-XXO) & ACCESS
- K871573 — CENTRAL VENOUS MULTI-LUMEN CATHETERS AND KITS
- K865101 — SPECTRAMED MODEL SP1455 HEMOPRO2 SYSTEM
- K864507 — V-PACE(TM) TRANSLUMINAL VENTRICULAR/ MODEL SP5540
Data sourced from openFDA. This site is unofficial and independent of the FDA.