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FDA 510(k)

HANG UPS POWER II

K-Number: K991835 · 1999-12-20

ApplicantStl Intl., Inc.
Decision Date1999-12-20
Product CodeITH
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HANG UPS POWER II is the device name listed in this FDA 510(k) record. The listed applicant is Stl Intl., Inc.. It received FDA 510(k) clearance on 1999-12-20 under 510(k) number K991835. The device is classified under product code ITH. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANG UPS POWER II?

HANG UPS POWER II is a medical device that received FDA 510(k) clearance on 1999-12-20. The listed applicant is Stl Intl., Inc.. The 510(k) number is K991835.

When did HANG UPS POWER II receive FDA 510(k) clearance?

HANG UPS POWER II received FDA 510(k) clearance on 1999-12-20, under 510(k) number K991835.

Who is the listed applicant for HANG UPS POWER II?

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

What is the FDA product code for HANG UPS POWER II?

The FDA product code for HANG UPS POWER II is ITH.

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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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