PRO DISCS
K-Number: K882630 · 1989-02-16
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Device Summary
Frequently Asked Questions
What is the PRO DISCS?
PRO DISCS is a medical device that received FDA 510(k) clearance on 1989-02-16. The listed applicant is Carr-Scarborough Microbiologicals, Inc.. The 510(k) number is K882630.
When did PRO DISCS receive FDA 510(k) clearance?
PRO DISCS received FDA 510(k) clearance on 1989-02-16, under 510(k) number K882630.
Who is the listed applicant for PRO DISCS?
The FDA 510(k) record lists Carr-Scarborough Microbiologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRO DISCS?
The FDA product code for PRO DISCS is JTO.
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 Carr-Scarborough Microbiologicals, 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: JTO)
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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