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FDA 510(k)

PRO CHECK DIGITAL PACIFIER THERMOMETER

K-Number: K972259 · 1997-07-10

Decision Date1997-07-10
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRO CHECK DIGITAL PACIFIER THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Micro Weiss Electronics. It received FDA 510(k) clearance on 1997-07-10 under 510(k) number K972259. 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 PRO CHECK DIGITAL PACIFIER THERMOMETER?

PRO CHECK DIGITAL PACIFIER THERMOMETER is a medical device that received FDA 510(k) clearance on 1997-07-10. The listed applicant is Micro Weiss Electronics. The 510(k) number is K972259.

When did PRO CHECK DIGITAL PACIFIER THERMOMETER receive FDA 510(k) clearance?

PRO CHECK DIGITAL PACIFIER THERMOMETER received FDA 510(k) clearance on 1997-07-10, under 510(k) number K972259.

Who is the listed applicant for PRO CHECK DIGITAL PACIFIER THERMOMETER?

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

What is the FDA product code for PRO CHECK DIGITAL PACIFIER THERMOMETER?

The FDA product code for PRO CHECK DIGITAL PACIFIER THERMOMETER 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 Micro Weiss Electronics 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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