NUTRAC PELVATOR, MODEL PEL 200
K-Number: K083704 · 2009-07-14
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Device Summary
Frequently Asked Questions
What is the NUTRAC PELVATOR, MODEL PEL 200?
NUTRAC PELVATOR, MODEL PEL 200 is a medical device that received FDA 510(k) clearance on 2009-07-14. The listed applicant is Verity Scientific , Ltd.. The 510(k) number is K083704.
When did NUTRAC PELVATOR, MODEL PEL 200 receive FDA 510(k) clearance?
NUTRAC PELVATOR, MODEL PEL 200 received FDA 510(k) clearance on 2009-07-14, under 510(k) number K083704.
Who is the listed applicant for NUTRAC PELVATOR, MODEL PEL 200?
The FDA 510(k) record lists Verity Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NUTRAC PELVATOR, MODEL PEL 200?
The FDA product code for NUTRAC PELVATOR, MODEL PEL 200 is KPI.
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.
Related Devices (Code: KPI)
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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