NF DEVICE— 510(k) K770517

Substantially Equivalent

Rpr, Inc.

FDA 510(k) clearance K770517 for NF DEVICE, Substantially Equivalent on 1977-07-15. Applicant: Rpr, Inc.. Device class: 2.

Clearance details

Applicant: Rpr, Inc.
Product code: Code KPD
Device class: Class 2
Regulation: 21 CFR 880.2200
Advisory panel: General Hospital
Date received: 1977-03-18
Decision date: 1977-07-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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