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FDA 510(k)

MANAN ACCURA NEEDLE

K-Number: K974741 · 1998-01-08

ApplicantMedical Device Technologies, Inc.
Decision Date1998-01-08
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MANAN ACCURA NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1998-01-08 under 510(k) number K974741. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANAN ACCURA NEEDLE?

MANAN ACCURA NEEDLE is a medical device that received FDA 510(k) clearance on 1998-01-08. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K974741.

When did MANAN ACCURA NEEDLE receive FDA 510(k) clearance?

MANAN ACCURA NEEDLE received FDA 510(k) clearance on 1998-01-08, under 510(k) number K974741.

Who is the listed applicant for MANAN ACCURA NEEDLE?

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

What is the FDA product code for MANAN ACCURA NEEDLE?

The FDA product code for MANAN ACCURA NEEDLE is GAA.

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Related Devices (Code: GAA)

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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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