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FDA 510(k)

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER

K-Number: K040034 · 2004-02-11

ApplicantBlackstone Medical, Inc.
Decision Date2004-02-11
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Blackstone Medical, Inc.. It received FDA 510(k) clearance on 2004-02-11 under 510(k) number K040034. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER?

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER is a medical device that received FDA 510(k) clearance on 2004-02-11. The listed applicant is Blackstone Medical, Inc.. The 510(k) number is K040034.

When did BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER receive FDA 510(k) clearance?

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER received FDA 510(k) clearance on 2004-02-11, under 510(k) number K040034.

Who is the listed applicant for BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER?

The FDA 510(k) record lists Blackstone Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER?

The FDA product code for BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER is MNI.

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Related Devices (Code: MNI)

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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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