VERSATOME— 510(k) K771549

Substantially Equivalent

Kermath Mfg. Corp.

FDA 510(k) clearance K771549 for VERSATOME, Substantially Equivalent on 1977-08-25. Applicant: Kermath Mfg. Corp.. Device class: 2.

Clearance details

Applicant: Kermath Mfg. Corp.
Product code: Code IZF
Device class: Class 2
Regulation: 21 CFR 892.1740
Advisory panel: Radiology
Date received: 1977-08-12
Decision date: 1977-08-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code IZF

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K870221 — T.O.P. 2000 (TOMOGRAPHIC ORIENTATED PLANNING)1987-05-12
K812726 — KERMATH THERAPY SIMULATOR1981-11-05
K812332 — KERMATH L/C ARM1981-09-16
K811215 — KERMATH RADIOGRAPHIC HEAD STAND1981-06-12

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