Scissor - 1.5MM Probe Point, Angled

FDA 510(k) K760792 · V. Mueller O.V. Baxter Healthcare Corp.

Substantially Equivalent

510(k) numberK760792

Submission

Device name
Scissor - 1.5MM Probe Point, Angled
Applicant
V. Mueller O.V. Baxter Healthcare Corp.
Mchenry, IL, US
Received
October 7, 1976
Decision date
November 11, 1976
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DWS – Instruments, Surgical, Cardiovascular
Device class
Class I (low risk)
Regulation
21 CFR 870.4500
Specialty
Cardiovascular

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K962771Burke Congenital Thoracoscopy InstrumentsDWS · Traditional Pilling Weck, Inc.11/19/1996SE
K955689RNS Sterile, Disposable Digital Angiographic TrayDWS · Traditional Contour Fabricators of Florida, Inc.05/15/1996SE
K960139G.E. Sterile Angiographic TrayDWS · Traditional GE Medical Systems04/19/1996SESK
K960144G.E. Sterile CT Biopsy TrayDWS · Traditional GE Medical Systems04/15/1996SESK
K960143G.E. Sterile Digital Angiographic TrayDWS · Traditional GE Medical Systems04/09/1996SESK
K934727Replacement Parts for Cpi 6888 Lead TunnelerDWS · Traditional Cardiac Pacemakers, Inc.01/10/1994SE
K900379Hycult Diamond Coronary Bypass KnifeDWS · Traditional St. Jude Medical, Inc.03/19/1990SE
K896307Insulation PadDWS · Traditional Bio-Vascular, Inc.01/19/1990SE

More from Bio-Vascular, Inc.

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K771197Norton EndotrachealBTR · Traditional 08/16/1977SE
K771302Pfister-Schwartz Stone RetrieverFGO · Traditional 08/02/1977SE
K770959Bougie, Filiform, JacksonKBI · Traditional 06/14/1977SE
K770280Cord, Electrosurgical-Sterile & Dispos.KNS · Traditional 04/15/1977SE
K760851Converse Altar RetractorKAL · Traditional 03/10/1977SE
K761242Teflon Coated Resectoscope SheathFJL · Traditional 12/16/1976SE
K760273LithotriteFGK · Traditional 12/06/1976SE
K760189Stopcock, WaterlineFAJ · Traditional 12/02/1976SE

Questions and answers

When was Scissor - 1.5MM Probe Point, Angled cleared by the FDA?

Scissor - 1.5MM Probe Point, Angled (K760792) received a 510(k) decision of Substantially Equivalent on November 11, 1976, 35 days after the submission was received.

What is the product code of K760792?

The FDA product code is DWS – Instruments, Surgical, Cardiovascular, a Class I (low risk) device regulated under 21 CFR 870.4500.