FDA 510(k)

SIMS SILO NEEDLE DE-ACCESS ENCLOSURE

K-Number: K935767 · 1995-11-15

Decision Date1995-11-15

Product CodeLJT

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

SIMS SILO NEEDLE DE-ACCESS ENCLOSURE is the device name listed in this FDA 510(k) record. The listed applicant is Sims Deltec, Inc.. It received FDA 510(k) clearance on 1995-11-15 under 510(k) number K935767. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMS SILO NEEDLE DE-ACCESS ENCLOSURE?

SIMS SILO NEEDLE DE-ACCESS ENCLOSURE is a medical device that received FDA 510(k) clearance on 1995-11-15. The listed applicant is Sims Deltec, Inc.. The 510(k) number is K935767.

When did SIMS SILO NEEDLE DE-ACCESS ENCLOSURE receive FDA 510(k) clearance?

SIMS SILO NEEDLE DE-ACCESS ENCLOSURE received FDA 510(k) clearance on 1995-11-15, under 510(k) number K935767.

Who is the listed applicant for SIMS SILO NEEDLE DE-ACCESS ENCLOSURE?

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

What is the FDA product code for SIMS SILO NEEDLE DE-ACCESS ENCLOSURE?

The FDA product code for SIMS SILO NEEDLE DE-ACCESS ENCLOSURE is LJT.

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Other records listing Sims Deltec, Inc. as applicant

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Related Devices (Code: LJT)

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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.