CENTRIX PCR MOLAR MATRIX FORMS (BANDS)
K-Number: K861581 · 1986-05-12
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Device Summary
Frequently Asked Questions
What is the CENTRIX PCR MOLAR MATRIX FORMS (BANDS)?
CENTRIX PCR MOLAR MATRIX FORMS (BANDS) is a medical device that received FDA 510(k) clearance on 1986-05-12. The listed applicant is Centrix, Inc.. The 510(k) number is K861581.
When did CENTRIX PCR MOLAR MATRIX FORMS (BANDS) receive FDA 510(k) clearance?
CENTRIX PCR MOLAR MATRIX FORMS (BANDS) received FDA 510(k) clearance on 1986-05-12, under 510(k) number K861581.
Who is the listed applicant for CENTRIX PCR MOLAR MATRIX FORMS (BANDS)?
The FDA 510(k) record lists Centrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRIX PCR MOLAR MATRIX FORMS (BANDS)?
The FDA product code for CENTRIX PCR MOLAR MATRIX FORMS (BANDS) is DZN.
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 Centrix, 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: DZN)
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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