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FDA 510(k)

TRIANGLE SLING

K-Number: K980482 · 1998-03-27

ApplicantInfluence, Inc.
Decision Date1998-03-27
Product CodeOTN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TRIANGLE SLING is the device name listed in this FDA 510(k) record. The listed applicant is Influence, Inc.. It received FDA 510(k) clearance on 1998-03-27 under 510(k) number K980482. 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 TRIANGLE SLING?

TRIANGLE SLING is a medical device that received FDA 510(k) clearance on 1998-03-27. The listed applicant is Influence, Inc.. The 510(k) number is K980482.

When did TRIANGLE SLING receive FDA 510(k) clearance?

TRIANGLE SLING received FDA 510(k) clearance on 1998-03-27, under 510(k) number K980482.

Who is the listed applicant for TRIANGLE SLING?

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

What is the FDA product code for TRIANGLE SLING?

The FDA product code for TRIANGLE SLING is OTN.

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Related Devices (Code: OTN)

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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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