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FDA 510(k)

PACIFIER THERMOMETER MODELS VT-901F, VT901C

K-Number: K002562 · 2000-10-13

ApplicantValeo Corp.
Decision Date2000-10-13
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PACIFIER THERMOMETER MODELS VT-901F, VT901C is the device name listed in this FDA 510(k) record. The listed applicant is Valeo Corp.. It received FDA 510(k) clearance on 2000-10-13 under 510(k) number K002562. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACIFIER THERMOMETER MODELS VT-901F, VT901C?

PACIFIER THERMOMETER MODELS VT-901F, VT901C is a medical device that received FDA 510(k) clearance on 2000-10-13. The listed applicant is Valeo Corp.. The 510(k) number is K002562.

When did PACIFIER THERMOMETER MODELS VT-901F, VT901C receive FDA 510(k) clearance?

PACIFIER THERMOMETER MODELS VT-901F, VT901C received FDA 510(k) clearance on 2000-10-13, under 510(k) number K002562.

Who is the listed applicant for PACIFIER THERMOMETER MODELS VT-901F, VT901C?

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

What is the FDA product code for PACIFIER THERMOMETER MODELS VT-901F, VT901C?

The FDA product code for PACIFIER THERMOMETER MODELS VT-901F, VT901C is FLL.

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.

Other records listing Valeo Corp. as applicant

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: FLL)

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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