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FDA 510(k)

PELVIMESH / HERMESH 7

K-Number: K070625 · 2007-08-01

ApplicantMarketing Solutions, Inc.
Decision Date2007-08-01
Product CodeFTL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PELVIMESH / HERMESH 7 is the device name listed in this FDA 510(k) record. The listed applicant is Marketing Solutions, Inc.. It received FDA 510(k) clearance on 2007-08-01 under 510(k) number K070625. The device is classified under product code FTL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PELVIMESH / HERMESH 7?

PELVIMESH / HERMESH 7 is a medical device that received FDA 510(k) clearance on 2007-08-01. The listed applicant is Marketing Solutions, Inc.. The 510(k) number is K070625.

When did PELVIMESH / HERMESH 7 receive FDA 510(k) clearance?

PELVIMESH / HERMESH 7 received FDA 510(k) clearance on 2007-08-01, under 510(k) number K070625.

Who is the listed applicant for PELVIMESH / HERMESH 7?

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

What is the FDA product code for PELVIMESH / HERMESH 7?

The FDA product code for PELVIMESH / HERMESH 7 is FTL.

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Related Devices (Code: FTL)

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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