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FDA 510(k)

IN-SLING

K-Number: K972651 · 1997-09-19

ApplicantInfluence, Inc.
Decision Date1997-09-19
Product CodeOTN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IN-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 1997-09-19 under 510(k) number K972651. 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 IN-SLING?

IN-SLING is a medical device that received FDA 510(k) clearance on 1997-09-19. The listed applicant is Influence, Inc.. The 510(k) number is K972651.

When did IN-SLING receive FDA 510(k) clearance?

IN-SLING received FDA 510(k) clearance on 1997-09-19, under 510(k) number K972651.

Who is the listed applicant for IN-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 IN-SLING?

The FDA product code for IN-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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