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FDA 510(k)

DESARA MESH SLING, MODEL CAL-DS01

K-Number: K072456 · 2008-05-08

Decision Date2008-05-08
Product CodeOTN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DESARA MESH SLING, MODEL CAL-DS01 is the device name listed in this FDA 510(k) record. The listed applicant is Caldera Medical, Inc.. It received FDA 510(k) clearance on 2008-05-08 under 510(k) number K072456. 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 DESARA MESH SLING, MODEL CAL-DS01?

DESARA MESH SLING, MODEL CAL-DS01 is a medical device that received FDA 510(k) clearance on 2008-05-08. The listed applicant is Caldera Medical, Inc.. The 510(k) number is K072456.

When did DESARA MESH SLING, MODEL CAL-DS01 receive FDA 510(k) clearance?

DESARA MESH SLING, MODEL CAL-DS01 received FDA 510(k) clearance on 2008-05-08, under 510(k) number K072456.

Who is the listed applicant for DESARA MESH SLING, MODEL CAL-DS01?

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

What is the FDA product code for DESARA MESH SLING, MODEL CAL-DS01?

The FDA product code for DESARA MESH SLING, MODEL CAL-DS01 is OTN.

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.

Other records listing Caldera Medical, 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.

View all 20 devices →

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.

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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