PARALLEL BLADE MARKER— 510(k) K780991

Name: FDA 510(k) clearance K780991
Creator: U.S. Food and Drug Administration
Published: 1978-10-03

Substantially Equivalent

Nestor Engineering Associates, Inc.

FDA 510(k) clearance K780991 for PARALLEL BLADE MARKER, Substantially Equivalent on 1978-10-03. Applicant: Nestor Engineering Associates, Inc.. Device class: 1.

Clearance details

Applicant: Nestor Engineering Associates, Inc.
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1978-06-14
Decision date: 1978-10-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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