Disposable Patient Cable Model 5807

FDA 510(k) K801064 · Daig Corp.

Substantially Equivalent

510(k) numberK801064

Submission

Device name
Disposable Patient Cable Model 5807
Applicant
Daig Corp.
Mchenry, IL, US
Received
May 6, 1980
Decision date
May 14, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DSA – Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2900
Specialty
Cardiovascular

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Questions and answers

When was Disposable Patient Cable Model 5807 cleared by the FDA?

Disposable Patient Cable Model 5807 (K801064) received a 510(k) decision of Substantially Equivalent on May 14, 1980, 8 days after the submission was received.

What is the product code of K801064?

The FDA product code is DSA – Cable, Transducer And Electrode, Patient, (Including Connector), a Class II (moderate risk) device regulated under 21 CFR 870.2900.