Disposable Microtome Blade

FDA 510(k) K831308 · Surgipath Medical Industries, Inc.

Substantially Equivalent

510(k) numberK831308

Submission

Device name
Disposable Microtome Blade
Applicant
Surgipath Medical Industries, Inc.
Mchenry, IL, US
Received
April 22, 1983
Decision date
May 16, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IDL – Microtome, Accessories
Device class
Class I (low risk)
Regulation
21 CFR 864.3010
Specialty
Pathology

Other 510(k)s with product code IDL

510(k)DeviceApplicantDecision
K863616Knife MakerIDL · Traditional Surgipath Medical Industries, Inc.09/25/1986SE
K831921Disposable Microtome BladesIDL · Traditional Polymer Technology Corp.07/29/1983SE
K813430Tissue Processing Cassettes & AccessIDL · Traditional American Optical Corp.12/29/1981SE
K801426Tissue-Tek III Microject Disp. Blade SysIDL · Traditional Miles Laboratories, Inc.07/28/1980SE

More from Miles Laboratories, Inc.

510(k)DeviceDecision
K883217Schiff ReagentHZT · Traditional 08/05/1988SE
K881921C-E BrushHHT · Traditional 07/19/1988SE
K881922Cytojars Prefilled with Cytology PreservativeLDZ · Traditional 05/25/1988SE
K881659Tissue Section AdhesiveIFZ · Traditional 04/21/1988SE
K863549Reusable/Disposable Autopsy Knife SetEMF · Traditional 09/30/1986SE
K863616Knife MakerIDL · Traditional 09/25/1986SE
K863548Rotary MicrotomeIDO · Traditional 09/19/1986SE
K863483Cassette EmbosseerIDZ · Traditional 09/16/1986SE
K863145Cervical ScrapersHHT · Traditional 08/19/1986SE
K861270Blue Ribbon Paraffin Infiltration/Embedding Med.KEO · Traditional 04/11/1986SE

Questions and answers

When was Disposable Microtome Blade cleared by the FDA?

Disposable Microtome Blade (K831308) received a 510(k) decision of Substantially Equivalent on May 16, 1983, 24 days after the submission was received.

What is the product code of K831308?

The FDA product code is IDL – Microtome, Accessories, a Class I (low risk) device regulated under 21 CFR 864.3010.