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FDA 510(k)

AIM-V (R) MEDIUM, MODEL 087-0112

K-Number: K022086 · 2002-12-23

ApplicantInvitrogen Corporation
Decision Date2002-12-23
Product CodeNDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

AIM-V (R) MEDIUM, MODEL 087-0112 is the device name listed in this FDA 510(k) record. The listed applicant is Invitrogen Corporation. It received FDA 510(k) clearance on 2002-12-23 under 510(k) number K022086. The device is classified under product code NDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIM-V (R) MEDIUM, MODEL 087-0112?

AIM-V (R) MEDIUM, MODEL 087-0112 is a medical device that received FDA 510(k) clearance on 2002-12-23. The listed applicant is Invitrogen Corporation. The 510(k) number is K022086.

When did AIM-V (R) MEDIUM, MODEL 087-0112 receive FDA 510(k) clearance?

AIM-V (R) MEDIUM, MODEL 087-0112 received FDA 510(k) clearance on 2002-12-23, under 510(k) number K022086.

Who is the listed applicant for AIM-V (R) MEDIUM, MODEL 087-0112?

The FDA 510(k) record lists Invitrogen Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIM-V (R) MEDIUM, MODEL 087-0112?

The FDA product code for AIM-V (R) MEDIUM, MODEL 087-0112 is NDS.

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Related Devices (Code: NDS)

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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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