THE SPANTRON FRAME FREEZE— 510(k) K890477

Substantially Equivalent

Spantron, Inc.

FDA 510(k) clearance K890477 for THE SPANTRON FRAME FREEZE, Substantially Equivalent on 1989-03-31. Applicant: Spantron, Inc.. Device class: 2.

Clearance details

Applicant: Spantron, Inc.
Product code: Code LMA
Device class: Class 2
Regulation: 21 CFR 892.2030
Advisory panel: Radiology
Date received: 1989-01-31
Decision date: 1989-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

Download summary PDF View on FDA.gov ↗

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More clearances from Spantron, Inc.

K895546 — MODIFIED SPANTRON FRAME FREEZE1989-11-13

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