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FDA 510(k)

R&D SICKLE QC CONTROL

K-Number: K070334 · 2007-03-29

ApplicantR&D Systems, Inc.
Decision Date2007-03-29
Product CodeGGM
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

R&D SICKLE QC CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is R&D Systems, Inc.. It received FDA 510(k) clearance on 2007-03-29 under 510(k) number K070334. The device is classified under product code GGM. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the R&D SICKLE QC CONTROL?

R&D SICKLE QC CONTROL is a medical device that received FDA 510(k) clearance on 2007-03-29. The listed applicant is R&D Systems, Inc.. The 510(k) number is K070334.

When did R&D SICKLE QC CONTROL receive FDA 510(k) clearance?

R&D SICKLE QC CONTROL received FDA 510(k) clearance on 2007-03-29, under 510(k) number K070334.

Who is the listed applicant for R&D SICKLE QC CONTROL?

The FDA 510(k) record lists R&D Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for R&D SICKLE QC CONTROL?

The FDA product code for R&D SICKLE QC CONTROL is GGM.

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Related Devices (Code: GGM)

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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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