Egnell Compact Suction Pump

FDA 510(k) K853917 · Egnell, Inc.

Substantially Equivalent for Some Indications

510(k) numberK853917

Submission

Device name
Egnell Compact Suction Pump
Applicant
Egnell, Inc.
Chicago, IL, US
Received
September 23, 1985
Decision date
November 25, 1985
Decision
Substantially Equivalent for Some Indications (SN)
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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More from Shenzhen Kingboom Technology Co., Ltd.

510(k)DeviceDecision
K853909Egnell Universal Suction PumpBTA · Traditional 11/25/1985SN
K844307Egnell-Lact B Battery-Operated Breast PumpHGX · Traditional 02/04/1985SE
K840526AmethermFMZ · Traditional 04/30/1984SE
K834335Ameda Phototherapy Lamp for NewbornLBI · Traditional 04/20/1984SE
K832637Ameda Neonatal Resuscitation Unit-FMT · Traditional 12/22/1983SE
K813312Universal Suction Pump Type EusBTA · Traditional 12/31/1981SE
K813095Gastric Juices Suction PumpBTA · Traditional 12/09/1981SE
K812898PE-01 Electronic Infusion PumpFRN · Traditional 12/02/1981SE
K812020Egnell Compact, Type EhvBTA · Traditional 10/20/1981SE

Questions and answers

When was Egnell Compact Suction Pump cleared by the FDA?

Egnell Compact Suction Pump (K853917) received a 510(k) decision of Substantially Equivalent for Some Indications on November 25, 1985, 63 days after the submission was received.

What is the product code of K853917?

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