GEISTER SURGICAL INT'L MONOPOLAR ENDOSCOPIC SURG.INST.— 510(k) K933300

Name: FDA 510(k) clearance K933300
Creator: U.S. Food and Drug Administration
Published: 1994-09-30

Substantially Equivalent

Lyle Howard Corp.

FDA 510(k) clearance K933300 for GEISTER SURGICAL INT'L MONOPOLAR ENDOSCOPIC SURG.INST., Substantially Equivalent on 1994-09-30. Applicant: Lyle Howard Corp.. Device class: 2.

Clearance details

Applicant: Lyle Howard Corp.
Product code: Product code KNF
Device class: Class 2
Regulation: 21 CFR 884.4160
Advisory panel: Obstetrics/Gynecology
Date received: 1993-07-07
Decision date: 1994-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lebanon, NJ, US

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