S-Scort (2500)

FDA 510(k) K964997 · Sscor

Substantially Equivalent

510(k) numberK964997

Submission

Device name
S-Scort (2500)
Applicant
Sscor
Sun Valley, CA, US
Received
December 16, 1996
Decision date
March 5, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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More from Shenzhen Kingboom Technology Co., Ltd.

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K950464Sscor/Board ..3 Model 23000 Pre-Assembled Suction System for Patient Transport VehiclesGCX · Traditional 04/25/1995SE
K945929S-Scort(R)Duet Model 2014 Portable Suction PumpBTA · Traditional 12/22/1994SE

Questions and answers

When was S-Scort (2500) cleared by the FDA?

S-Scort (2500) (K964997) received a 510(k) decision of Substantially Equivalent on March 5, 1997, 79 days after the submission was received.

What is the product code of K964997?

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