GETTIG STYRL-JECT DELIVERY SYSTEM— 510(k) K972285

Name: FDA 510(k) clearance K972285
Creator: U.S. Food and Drug Administration
Published: 1997-09-11

Substantially Equivalent

Gettig Pharmaceutical Instrument Co.

FDA 510(k) clearance K972285 for GETTIG STYRL-JECT DELIVERY SYSTEM, Substantially Equivalent on 1997-09-11. Applicant: Gettig Pharmaceutical Instrument Co.. Device class: 2.

Clearance details

Applicant: Gettig Pharmaceutical Instrument Co.
Product code: Code EJI
Device class: Class 2
Regulation: 21 CFR 872.6770
Advisory panel: Dental
Date received: 1997-06-19
Decision date: 1997-09-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spring Mills, PA, US

Download summary PDF View on FDA.gov ↗

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