Chlamydia Transettee 1 & 3

FDA 510(k) K823179 · Spectrum Co.

Substantially Equivalent

510(k) numberK823179

Submission

Device name
Chlamydia Transettee 1 & 3
Applicant
Spectrum Co.
Mchenry, IL, US
Received
October 26, 1982
Decision date
November 16, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSM – Culture Media, Non-Propagating Transport
Device class
Class I (low risk)
Regulation
21 CFR 866.2390
Specialty
Microbiology

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Questions and answers

When was Chlamydia Transettee 1 & 3 cleared by the FDA?

Chlamydia Transettee 1 & 3 (K823179) received a 510(k) decision of Substantially Equivalent on November 16, 1982, 21 days after the submission was received.

What is the product code of K823179?

The FDA product code is JSM – Culture Media, Non-Propagating Transport, a Class I (low risk) device regulated under 21 CFR 866.2390.