Kit, Prep Shave

FDA 510(k) K760052 · M-C Ind., Inc.

Substantially Equivalent

510(k) numberK760052

Submission

Device name
Kit, Prep Shave
Applicant
M-C Ind., Inc.
Mchenry, IL, US
Received
June 15, 1976
Decision date
July 16, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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K981032Piv SystemLDQ · Traditional Medical Solutions, Inc.09/02/1998SE
K973747Controlled Temperature Cabinet SystemLDQ · Traditional Smith05/07/1998SE
K955661Acu-HaltLDQ · Traditional Glederer & Co., Inc.12/30/1996SE
K955776Acu-LabLDQ · Traditional Glederer & Co., Inc.06/05/1996SE
K945374Acu-HaltLDQ · Traditional Eva-Health USA, Inc.08/09/1995SE
K944961Personal Alarm System (Pas)LDQ · Traditional Cytoprobe Corp.08/07/1995SE
K942810Palco Labs Cold PouchLDQ · Traditional Palco Laboratories, Inc.06/28/1995SE
K930884Medical Procedure Tray, ModificationLDQ · Traditional Enpak Medical Corp.03/21/1995SE

More from Enpak Medical Corp.

510(k)DeviceDecision
K760048Tray, Urethral CatheterizationFCM · Traditional 03/01/1977SE
K760047Tray, Bladder IrrigationEYN · Traditional 03/01/1977SE
K760051Tray, Suture RemovalKDD · Traditional 08/30/1976SE

Questions and answers

When was Kit, Prep Shave cleared by the FDA?

Kit, Prep Shave (K760052) received a 510(k) decision of Substantially Equivalent on July 16, 1976, 31 days after the submission was received.