Egnell Compact, Type Ehv

FDA 510(k) K812020 · Egnell, Inc.

Substantially Equivalent

510(k) numberK812020

Submission

Device name
Egnell Compact, Type Ehv
Applicant
Egnell, Inc.
Mchenry, IL, US
Received
July 20, 1981
Decision date
October 20, 1981
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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More from Shenzhen Kingboom Technology Co., Ltd.

510(k)DeviceDecision
K853917Egnell Compact Suction PumpBTA · Traditional 11/25/1985SN
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

Questions and answers

When was Egnell Compact, Type Ehv cleared by the FDA?

Egnell Compact, Type Ehv (K812020) received a 510(k) decision of Substantially Equivalent on October 20, 1981, 92 days after the submission was received.

What is the product code of K812020?

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