JOHNSON & JOHNSON FLUFF SPONGE— 510(k) K881222

Name: FDA 510(k) clearance K881222
Creator: U.S. Food and Drug Administration
Published: 1988-03-28

Substantially Equivalent

Johnson & Johnson Professionals, Inc.

FDA 510(k) clearance K881222 for JOHNSON & JOHNSON FLUFF SPONGE, Substantially Equivalent on 1988-03-28. Applicant: Johnson & Johnson Professionals, Inc.. Device class: Unclassified.

Clearance details

Applicant: Johnson & Johnson Professionals, Inc.
Product code: Code EFQ
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-03-22
Decision date: 1988-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raynham, MA, 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.