GP3%SP-2100DOHON100/120 Mesh Supelcoport

FDA 510(k) K761226 · Supelco, Inc.

Substantially Equivalent

510(k) numberK761226

Submission

Device name
GP3%SP-2100DOHON100/120 Mesh Supelcoport
Applicant
Supelco, Inc.
Mchenry, IL, US
Received
December 9, 1976
Decision date
January 14, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JSQ – Chromatography For Bacterial Identification
Device class
Class I (low risk)
Regulation
21 CFR 862.2250
Specialty
Clinical Chemistry

Other 510(k)s with product code JSQ

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K834007Cystine Tryptic MediumJSQ · Traditional Micro Media Laboratories12/22/1983SE
K811138Nutrient AgarJSQ · Traditional Acumedia Manufacturers, Inc.05/05/1981SE

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Questions and answers

When was GP3%SP-2100DOHON100/120 Mesh Supelcoport cleared by the FDA?

GP3%SP-2100DOHON100/120 Mesh Supelcoport (K761226) received a 510(k) decision of Substantially Equivalent on January 14, 1977, 36 days after the submission was received.

What is the product code of K761226?

The FDA product code is JSQ – Chromatography For Bacterial Identification, a Class I (low risk) device regulated under 21 CFR 862.2250.