HEMO-WEDGE— 510(k) K790555

Substantially Equivalent

Parker Laboratories, Inc.

FDA 510(k) clearance K790555 for HEMO-WEDGE, Substantially Equivalent on 1980-01-17. Applicant: Parker Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Parker Laboratories, Inc.
Product code: Code DZN
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1979-03-19
Decision date: 1980-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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