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FDA 510(k)

MINI-TONG

K-Number: K101101 · 2010-07-23

ApplicantMini Lap Technologies, Inc.
Decision Date2010-07-23
Product CodeOCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MINI-TONG is the device name listed in this FDA 510(k) record. The listed applicant is Mini Lap Technologies, Inc.. It received FDA 510(k) clearance on 2010-07-23 under 510(k) number K101101. 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 MINI-TONG?

MINI-TONG is a medical device that received FDA 510(k) clearance on 2010-07-23. The listed applicant is Mini Lap Technologies, Inc.. The 510(k) number is K101101.

When did MINI-TONG receive FDA 510(k) clearance?

MINI-TONG received FDA 510(k) clearance on 2010-07-23, under 510(k) number K101101.

Who is the listed applicant for MINI-TONG?

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

What is the FDA product code for MINI-TONG?

The FDA product code for MINI-TONG is OCW.

Other records listing Mini Lap Technologies, Inc. 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.

K093449MINI LAP RETRACTORSK083754MINI LAP ELECTROCAUTERY INSTRUMENTSK070686MINI LAP INSTRUMENTSK070352MINI LAP PEDIATRIC INSTRUMENTS WITH MEDUSA CLAMPING SYSTEM

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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