FDA 510(k)

REPROCESSED STONE RETRIEVAL BASKETS

K-Number: K012581 · 2002-02-14

Decision Date2002-02-14

Product CodeFFL

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

REPROCESSED STONE RETRIEVAL BASKETS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2002-02-14 under 510(k) number K012581. The device is classified under product code FFL. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED STONE RETRIEVAL BASKETS?

REPROCESSED STONE RETRIEVAL BASKETS is a medical device that received FDA 510(k) clearance on 2002-02-14. The listed applicant is Sterilmed, Inc.. The 510(k) number is K012581.

When did REPROCESSED STONE RETRIEVAL BASKETS receive FDA 510(k) clearance?

REPROCESSED STONE RETRIEVAL BASKETS received FDA 510(k) clearance on 2002-02-14, under 510(k) number K012581.

Who is the listed applicant for REPROCESSED STONE RETRIEVAL BASKETS?

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

What is the FDA product code for REPROCESSED STONE RETRIEVAL BASKETS?

The FDA product code for REPROCESSED STONE RETRIEVAL BASKETS is FFL.

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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.