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FDA 510(k)

NATUS WARMETTE BLANKET AND DUAL CABINETS

K-Number: K132110 · 2013-10-03

ApplicantNatus Nicolet Ireland, Ltd.
Decision Date2013-10-03
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NATUS WARMETTE BLANKET AND DUAL CABINETS is the device name listed in this FDA 510(k) record. The listed applicant is Natus Nicolet Ireland, Ltd.. It received FDA 510(k) clearance on 2013-10-03 under 510(k) number K132110. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATUS WARMETTE BLANKET AND DUAL CABINETS?

NATUS WARMETTE BLANKET AND DUAL CABINETS is a medical device that received FDA 510(k) clearance on 2013-10-03. The listed applicant is Natus Nicolet Ireland, Ltd.. The 510(k) number is K132110.

When did NATUS WARMETTE BLANKET AND DUAL CABINETS receive FDA 510(k) clearance?

NATUS WARMETTE BLANKET AND DUAL CABINETS received FDA 510(k) clearance on 2013-10-03, under 510(k) number K132110.

Who is the listed applicant for NATUS WARMETTE BLANKET AND DUAL CABINETS?

The FDA 510(k) record lists Natus Nicolet Ireland, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NATUS WARMETTE BLANKET AND DUAL CABINETS?

The FDA product code for NATUS WARMETTE BLANKET AND DUAL CABINETS is LGZ.

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Related Devices (Code: LGZ)

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.

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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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