Jacobs High Vacuum Suction Unit 05-2570

FDA 510(k) K843693 · J. Sklar Mfg. Co., Inc.

Substantially Equivalent

510(k) numberK843693

Submission

Device name
Jacobs High Vacuum Suction Unit 05-2570
Applicant
J. Sklar Mfg. Co., Inc.
Long Island City, NY, US
Received
September 19, 1984
Decision date
October 31, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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K801273Magill Catheter Intro. ForcepsKOA · Traditional 07/28/1980SE
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K790577Hemorrhoidal LigatorHCF · Traditional 04/23/1979SE
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Questions and answers

When was Jacobs High Vacuum Suction Unit 05-2570 cleared by the FDA?

Jacobs High Vacuum Suction Unit 05-2570 (K843693) received a 510(k) decision of Substantially Equivalent on October 31, 1984, 42 days after the submission was received.

What is the product code of K843693?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.