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FDA 510(k)

SURGICAL DRAPE KIT - D.I.R.R.A. SRL

K-Number: K041080 · 2004-11-30

Decision Date2004-11-30
Product CodeLRO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL DRAPE KIT - D.I.R.R.A. SRL is the device name listed in this FDA 510(k) record. The listed applicant is D.I.R.R.A. S.R.L.. It received FDA 510(k) clearance on 2004-11-30 under 510(k) number K041080. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL DRAPE KIT - D.I.R.R.A. SRL?

SURGICAL DRAPE KIT - D.I.R.R.A. SRL is a medical device that received FDA 510(k) clearance on 2004-11-30. The listed applicant is D.I.R.R.A. S.R.L.. The 510(k) number is K041080.

When did SURGICAL DRAPE KIT - D.I.R.R.A. SRL receive FDA 510(k) clearance?

SURGICAL DRAPE KIT - D.I.R.R.A. SRL received FDA 510(k) clearance on 2004-11-30, under 510(k) number K041080.

Who is the listed applicant for SURGICAL DRAPE KIT - D.I.R.R.A. SRL?

The FDA 510(k) record lists D.I.R.R.A. S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SURGICAL DRAPE KIT - D.I.R.R.A. SRL?

The FDA product code for SURGICAL DRAPE KIT - D.I.R.R.A. SRL is LRO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: LRO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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