Volu-Sol Carnoy Fluid

FDA 510(k) K822126 · Volu Sol Medical Industries

Substantially Equivalent

510(k) numberK822126

Submission

Device name
Volu-Sol Carnoy Fluid
Applicant
Volu Sol Medical Industries
Mchenry, IL, US
Received
July 19, 1982
Decision date
August 5, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
IGM – Solution, Carnoy'S
Device class
Class I (low risk)
Regulation
21 CFR 864.4010
Specialty
Pathology

Other 510(k)s with product code IGM

510(k)DeviceApplicantDecision
K842737Carnoy's SolutionIGM · Traditional E K Ind., Inc.09/07/1984SE
K790815Culturette Brand PvaIGM · Traditional Marion Laboratories, Inc.05/15/1979SE

More from Marion Laboratories, Inc.

510(k)DeviceDecision
K822129Volu-Sol Bovins FixativeIGN · Traditional 08/05/1982SE
K822128Volu-Sol Single Differential StainICN · Traditional 08/05/1982SE
K822127Volu-Sol Zenkers FixativeIFH · Traditional 08/05/1982SE
K822038Volu-Sol Orange G-6(GILLS-MODHZH · Traditional 08/03/1982SE
K822037Volu-Sol Tap Water SubstitutePPM · Traditional 08/03/1982SE
K822036Volu-Sol DecalciferKDX · Traditional 08/03/1982SE
K822035Volu-Sol Gills EaHZJ · Traditional 08/03/1982SE
K812906Elvi Biclot 816KQG · Traditional 07/22/1982SE
K821541Hematoxylin IIIHYJ · Traditional 06/10/1982SE
K821540Hematoxylin IIHYJ · Traditional 06/10/1982SE

Questions and answers

When was Volu-Sol Carnoy Fluid cleared by the FDA?

Volu-Sol Carnoy Fluid (K822126) received a 510(k) decision of Substantially Equivalent on August 5, 1982, 17 days after the submission was received.

What is the product code of K822126?

The FDA product code is IGM – Solution, Carnoy'S, a Class I (low risk) device regulated under 21 CFR 864.4010.