Soluble Collagen

FDA 510(k) K780285 · General Diagnostics

Substantially Equivalent

510(k) numberK780285

Submission

Device name
Soluble Collagen
Applicant
General Diagnostics
Mchenry, IL, US
Received
February 21, 1978
Decision date
March 30, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JOZ – System, Automated Platelet Aggregation
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5700
Specialty
Hematology

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K833709Ceftizoxime 30 MCG Antimicrobial DiskJTN · Traditional 12/30/1983SE
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Questions and answers

When was Soluble Collagen cleared by the FDA?

Soluble Collagen (K780285) received a 510(k) decision of Substantially Equivalent on March 30, 1978, 37 days after the submission was received.

What is the product code of K780285?

The FDA product code is JOZ – System, Automated Platelet Aggregation, a Class II (moderate risk) device regulated under 21 CFR 864.5700.