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FDA 510(k)

MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM

K-Number: K132232 · 2013-12-04

ApplicantMinilap Technologies
Decision Date2013-12-04
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Minilap Technologies. It received FDA 510(k) clearance on 2013-12-04 under 510(k) number K132232. The device is classified under product code OCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM?

MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM is a medical device that received FDA 510(k) clearance on 2013-12-04. The listed applicant is Minilap Technologies. The 510(k) number is K132232.

When did MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM receive FDA 510(k) clearance?

MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM received FDA 510(k) clearance on 2013-12-04, under 510(k) number K132232.

Who is the listed applicant for MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM?

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

What is the FDA product code for MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM?

The FDA product code for MINS NEEDLESCOPIC RESPOSABLE DEVICE SYSTEM is OCW.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Minilap Technologies as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K113597MINI-LAP BIPOLAR ELECTROCAUTERY DEVICES

Related Devices (Code: OCW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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