VESSELOOPS— 510(k) K905240

Substantially Equivalent

Sparta Surgical Corp.

FDA 510(k) clearance K905240 for VESSELOOPS, Substantially Equivalent on 1991-02-06. Applicant: Sparta Surgical Corp.. Device class: 1.

Clearance details

Applicant: Sparta Surgical Corp.
Product code: Code KDC
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1990-11-20
Decision date: 1991-02-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hammonton, NJ, US

Download summary PDF View on FDA.gov ↗

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K920263 — MANUAL SURGICAL INSTRUMENTS1992-05-06
K915064 — DISPOSABLE CAUTERY ABRASIVE PAD1992-03-11

More clearances from Sparta Surgical Corp.

K965187 — SPECTRUM II, SPECTRUM PLUS, AND SPECTRUM MAX-SD1997-08-01
K945313 — SPARTA HYDROGEL WOUND DRESSING1995-01-12
K922729 — SPARTA WET DRESSING, SODIUM CHLORIDE1992-11-23
K905384 — DAVID SIMMONDS ANESTHESIA EXTENSION TUBES1991-03-22
K896085 — SURGI-BRUSH1989-11-08

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