Chamber V-9 Plus Agar

FDA 510(k) K851238 · Bug City Company, Inc.

Substantially Equivalent

510(k) numberK851238

Submission

Device name
Chamber V-9 Plus Agar
Applicant
Bug City Company, Inc.
Sapulpa, OK, US
Received
March 27, 1985
Decision date
May 29, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSJ – Culture Media, Selective And Non-Differential
Device class
Class I (low risk)
Regulation
21 CFR 866.2360
Specialty
Microbiology

Other 510(k)s with product code JSJ

510(k)DeviceApplicantDecision
K882463Potato Dextrose Agar (Pda) - Product #P3421JSJ · Traditional Lakewood Biochemical Co., Inc.06/22/1988SE
K881578StreptoselJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881574W-L Differential MediumJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881573Phytone Yeast Extract AgarJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881571Ym BrothJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881570Sabouraud Maltose AgarJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881565Inhibitory Mold AgarJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881561Tergitol 7 BrothJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881549Mycological Agar W/Low PHJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE
K881547Mitis Salivarius AgarJSJ · Traditional Acumedia Manufacturers, Inc.04/18/1988SE

Questions and answers

When was Chamber V-9 Plus Agar cleared by the FDA?

Chamber V-9 Plus Agar (K851238) received a 510(k) decision of Substantially Equivalent on May 29, 1985, 63 days after the submission was received.

What is the product code of K851238?

The FDA product code is JSJ – Culture Media, Selective And Non-Differential, a Class I (low risk) device regulated under 21 CFR 866.2360.