Cleared Traditional

GILL'S HEMATOXYLIN #3

K810760 · Surgipath · Pathology

Apr 1981

Decision

25d

Days

—

Risk

About This 510(k) Submission

K810760 is an FDA 510(k) clearance for the GILL'S HEMATOXYLIN #3, submitted by Surgipath (Mchenry, US). The FDA issued a Cleared decision on April 14, 1981, 25 days after receiving the submission on March 20, 1981. This device falls under the Pathology review panel.

Submission Details

510(k) Number	K810760 FDA.gov
FDA Decision	Cleared SESE
Date Received	March 20, 1981
Decision Date	April 14, 1981
Days to Decision	25 days
Submission Type	Traditional
Review Panel	Pathology (PA)
Summary	—