Cleared Traditional

K760621 - LANCER PLASTIC TRANSFER PIPETTE
(FDA 510(k) Clearance)

K760621 · Sherwood Medical Industries · Pathology device

Oct 1976

Decision

22d

Days

Class 1

Risk

K760621 is an FDA 510(k) clearance for the LANCER PLASTIC TRANSFER PIPETTE. This device is classified as a Micro Pipette (Class I - General Controls, product code JRC).

Submitted by Sherwood Medical Industries (Mchenry, US). The FDA issued a Cleared decision on October 5, 1976, 22 days after receiving the submission on September 13, 1976.

This device falls under the Pathology FDA review panel. Regulated under 21 CFR 862.2050.

Submission Details

510(k) Number	K760621 FDA.gov
FDA Decision	Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received	September 13, 1976
Decision Date	October 05, 1976
Days to Decision	22 days
Submission Type	Traditional
Review Panel	Pathology (PA)
Summary	—