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FDA 510(k)

PASTURE, MODELS: F550, A520

K-Number: K083176 · 2009-01-23

ApplicantPasture Pharma Pte, Ltd.
Decision Date2009-01-23
Product CodeNZJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PASTURE, MODELS: F550, A520 is the device name listed in this FDA 510(k) record. The listed applicant is Pasture Pharma Pte, Ltd.. It received FDA 510(k) clearance on 2009-01-23 under 510(k) number K083176. The device is classified under product code NZJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PASTURE, MODELS: F550, A520?

PASTURE, MODELS: F550, A520 is a medical device that received FDA 510(k) clearance on 2009-01-23. The listed applicant is Pasture Pharma Pte, Ltd.. The 510(k) number is K083176.

When did PASTURE, MODELS: F550, A520 receive FDA 510(k) clearance?

PASTURE, MODELS: F550, A520 received FDA 510(k) clearance on 2009-01-23, under 510(k) number K083176.

Who is the listed applicant for PASTURE, MODELS: F550, A520?

The FDA 510(k) record lists Pasture Pharma Pte, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PASTURE, MODELS: F550, A520?

The FDA product code for PASTURE, MODELS: F550, A520 is NZJ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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