PYRR MICROTUBE
K-Number: K812468 · 1981-09-14
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Device Summary
Frequently Asked Questions
What is the PYRR MICROTUBE?
PYRR MICROTUBE is a medical device that received FDA 510(k) clearance on 1981-09-14. The listed applicant is Carr Microbiologicals. The 510(k) number is K812468.
When did PYRR MICROTUBE receive FDA 510(k) clearance?
PYRR MICROTUBE received FDA 510(k) clearance on 1981-09-14, under 510(k) number K812468.
Who is the listed applicant for PYRR MICROTUBE?
The FDA 510(k) record lists Carr Microbiologicals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PYRR MICROTUBE?
The FDA product code for PYRR MICROTUBE is JSF.
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 Microbiologicals 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: JSF)
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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