Sorvall Embedding Medium

FDA 510(k) K760602 · E.I. Dupont DE Nemours & Co., Inc.

Substantially Equivalent

510(k) numberK760602

Submission

Device name
Sorvall Embedding Medium
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Mchenry, IL, US
Received
September 7, 1976
Decision date
September 21, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KEO – Formulations, Paraffin, All
Device class
Class I (low risk)
Regulation
21 CFR 864.4010
Specialty
Pathology

Other 510(k)s with product code KEO

510(k)DeviceApplicantDecision
K893772Tissue Embedding MediumKEO · Traditional Stephens Scientific06/22/1989SE
K862223Micro Thin* ParaffinKEO · Traditional Richard-Allan Medical Ind., Inc.06/17/1986SE
K862141Histology ParaffinKEO · Traditional Erie Scientific Co.06/13/1986SE
K861270Blue Ribbon Paraffin Infiltration/Embedding Med.KEO · Traditional Surgipath Medical Industries, Inc.04/11/1986SE
K842053Paraplast Extra Tissue Embedding Med.KEO · Traditional Sherwood Medical Co.06/26/1984SE
K833071Technicon ParacutKEO · Traditional Technicon Instruments Corp.10/14/1983SE
K831580Paraffin Infiltration MediumKEO · Traditional Surgipath Medical Industries, Inc.06/17/1983SE
K812191Vaspar SealentKEO · Traditional American Scientific Products08/31/1981SE
K810568Paraffin Embedding MediumKEO · Traditional Surgipath Medical Industries, Inc.03/17/1981SE
K803241Histological Embedding MediaKEO · Traditional Miles Laboratories, Inc.01/28/1981SE

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Questions and answers

When was Sorvall Embedding Medium cleared by the FDA?

Sorvall Embedding Medium (K760602) received a 510(k) decision of Substantially Equivalent on September 21, 1976, 14 days after the submission was received.

What is the product code of K760602?

The FDA product code is KEO – Formulations, Paraffin, All, a Class I (low risk) device regulated under 21 CFR 864.4010.