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FDA 510(k)

UNIMAX VERESS NEEDLE

K-Number: K111441 · 2011-08-19

ApplicantUnimax Medical Systems, Inc.
Decision Date2011-08-19
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNIMAX VERESS NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Unimax Medical Systems, Inc.. It received FDA 510(k) clearance on 2011-08-19 under 510(k) number K111441. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIMAX VERESS NEEDLE?

UNIMAX VERESS NEEDLE is a medical device that received FDA 510(k) clearance on 2011-08-19. The listed applicant is Unimax Medical Systems, Inc.. The 510(k) number is K111441.

When did UNIMAX VERESS NEEDLE receive FDA 510(k) clearance?

UNIMAX VERESS NEEDLE received FDA 510(k) clearance on 2011-08-19, under 510(k) number K111441.

Who is the listed applicant for UNIMAX VERESS NEEDLE?

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

What is the FDA product code for UNIMAX VERESS NEEDLE?

The FDA product code for UNIMAX VERESS NEEDLE is HIF.

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Other records listing Unimax Medical Systems, Inc. as applicant

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Related Devices (Code: HIF)

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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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