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FDA 510(k)

MENTOR OBTAPE TRANS-OBTURATOR TAPE

K-Number: K031767 · 2003-07-17

ApplicantMentor Corp.
Decision Date2003-07-17
Product CodeOTN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MENTOR OBTAPE TRANS-OBTURATOR TAPE is the device name listed in this FDA 510(k) record. The listed applicant is Mentor Corp.. It received FDA 510(k) clearance on 2003-07-17 under 510(k) number K031767. The device is classified under product code OTN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENTOR OBTAPE TRANS-OBTURATOR TAPE?

MENTOR OBTAPE TRANS-OBTURATOR TAPE is a medical device that received FDA 510(k) clearance on 2003-07-17. The listed applicant is Mentor Corp.. The 510(k) number is K031767.

When did MENTOR OBTAPE TRANS-OBTURATOR TAPE receive FDA 510(k) clearance?

MENTOR OBTAPE TRANS-OBTURATOR TAPE received FDA 510(k) clearance on 2003-07-17, under 510(k) number K031767.

Who is the listed applicant for MENTOR OBTAPE TRANS-OBTURATOR TAPE?

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

What is the FDA product code for MENTOR OBTAPE TRANS-OBTURATOR TAPE?

The FDA product code for MENTOR OBTAPE TRANS-OBTURATOR TAPE is OTN.

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Other records listing Mentor Corp. 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.

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Related Devices (Code: OTN)

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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