Seca Light Weight Baby Scale 744

FDA 510(k) K822042 · Seca Corp.

Substantially Equivalent

510(k) numberK822042

Submission

Device name
Seca Light Weight Baby Scale 744
Applicant
Seca Corp.
Mchenry, IL, US
Received
July 12, 1982
Decision date
July 28, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FRW – Scale, Patient
Device class
Class I (low risk)
Regulation
21 CFR 880.2720
Specialty
General Hospital

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K932572Digital Baby Scale Model BLB-12FRW · Traditional Tanita Corp. of America11/16/1993SE
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K926446Ez PumpFRW · Traditional Alphamed, Inc.09/27/1993SE
K9260593M Model 200RT Rate Taper Infusion PumpFRW · Traditional 3M Health Care, Ltd.08/16/1993SE
K9260583M Model 280RT Rate Taper Infusion PumpFRW · Traditional 3M Health Care, Ltd.08/16/1993SE

More from 3M Health Care, Ltd.

510(k)DeviceDecision
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K822135Seca Digital Baby Scale 727FRW · Traditional 07/30/1982SE
K822043Seca Chair SCALE-721FRW · Traditional 07/28/1982SE

Questions and answers

When was Seca Light Weight Baby Scale 744 cleared by the FDA?

Seca Light Weight Baby Scale 744 (K822042) received a 510(k) decision of Substantially Equivalent on July 28, 1982, 16 days after the submission was received.

What is the product code of K822042?

The FDA product code is FRW – Scale, Patient, a Class I (low risk) device regulated under 21 CFR 880.2720.