NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001— 510(k) K934368

Name: FDA 510(k) clearance K934368
Creator: U.S. Food and Drug Administration
Published: 1994-08-11

Substantially Equivalent

Nk Biotechnical Engineering Co.

FDA 510(k) clearance K934368 for NK PRESSURE-SPECIFIED SENSORY DEVICE, MODEL PSSD-001, Substantially Equivalent on 1994-08-11. Applicant: Nk Biotechnical Engineering Co.. Device class: 1.

Clearance details

Applicant: Nk Biotechnical Engineering Co.
Product code: Code LLN
Device class: Class 1
Regulation: 21 CFR 882.1200
Advisory panel: Neurology
Date received: 1993-09-07
Decision date: 1994-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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