VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16
K-Number: K062615 · 2007-01-29
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Device Summary
Frequently Asked Questions
What is the VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16?
VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16 is a medical device that received FDA 510(k) clearance on 2007-01-29. The listed applicant is Vision Biosystems, Inc.. The 510(k) number is K062615.
When did VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16 receive FDA 510(k) clearance?
VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16 received FDA 510(k) clearance on 2007-01-29, under 510(k) number K062615.
Who is the listed applicant for VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16?
The FDA 510(k) record lists Vision Biosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16?
The FDA product code for VISION BIOSYSTEMS PROGESTERONE RECEPTOR PGR CLONE 16 is MXZ.
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 Vision Biosystems, 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: MXZ)
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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