SPOR-TEST CULTURE MEDIA
K-Number: K801980 · 1980-09-09
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Device Summary
Frequently Asked Questions
What is the SPOR-TEST CULTURE MEDIA?
SPOR-TEST CULTURE MEDIA is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Mdt Corp., Inc.. The 510(k) number is K801980.
When did SPOR-TEST CULTURE MEDIA receive FDA 510(k) clearance?
SPOR-TEST CULTURE MEDIA received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801980.
Who is the listed applicant for SPOR-TEST CULTURE MEDIA?
The FDA 510(k) record lists Mdt Corp., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPOR-TEST CULTURE MEDIA?
The FDA product code for SPOR-TEST CULTURE MEDIA is JSG.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Mdt Corp., Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JSG)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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