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FDA 510(k)

MEDLINE PNEUMOPERITONEUM NEEDLE

K-Number: K111955 · 2011-11-16

ApplicantMedline Industries, Inc.
Decision Date2011-11-16
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDLINE PNEUMOPERITONEUM NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2011-11-16 under 510(k) number K111955. 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 MEDLINE PNEUMOPERITONEUM NEEDLE?

MEDLINE PNEUMOPERITONEUM NEEDLE is a medical device that received FDA 510(k) clearance on 2011-11-16. The listed applicant is Medline Industries, Inc.. The 510(k) number is K111955.

When did MEDLINE PNEUMOPERITONEUM NEEDLE receive FDA 510(k) clearance?

MEDLINE PNEUMOPERITONEUM NEEDLE received FDA 510(k) clearance on 2011-11-16, under 510(k) number K111955.

Who is the listed applicant for MEDLINE PNEUMOPERITONEUM NEEDLE?

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

What is the FDA product code for MEDLINE PNEUMOPERITONEUM NEEDLE?

The FDA product code for MEDLINE PNEUMOPERITONEUM NEEDLE is 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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