SURGITEK NPT MONITOR— 510(k) K875333

Substantially Equivalent

Surgitek

FDA 510(k) clearance K875333 for SURGITEK NPT MONITOR, Substantially Equivalent on 1988-04-13. Applicant: Surgitek. Device class: Unclassified.

Clearance details

Applicant: Surgitek
Product code: Code LIL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1987-12-30
Decision date: 1988-04-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Racine, WI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Surgitek

K946296 — QUADRA-COIL URETERAL STENT1995-03-06
K944391 — OM-4 (TENATIVE) URODYNAMIC MEASRUEMENT SYSTEM1995-02-07
K943491 — RIGHT ANGLE UROLOGIC LASER FIBER1994-08-05
K941952 — SURGITEK INFUSER1994-05-24
K933260 — HELICAL STONE/FLATWIRE STONE BASKETS1994-01-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.