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FDA 510(k)

QUICK CHECK INSTANT THERMOMETER

K-Number: K971831 · 1998-05-07

Decision Date1998-05-07
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

QUICK CHECK INSTANT THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Ejb Medical, Inc.. It received FDA 510(k) clearance on 1998-05-07 under 510(k) number K971831. 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 QUICK CHECK INSTANT THERMOMETER?

QUICK CHECK INSTANT THERMOMETER is a medical device that received FDA 510(k) clearance on 1998-05-07. The listed applicant is Ejb Medical, Inc.. The 510(k) number is K971831.

When did QUICK CHECK INSTANT THERMOMETER receive FDA 510(k) clearance?

QUICK CHECK INSTANT THERMOMETER received FDA 510(k) clearance on 1998-05-07, under 510(k) number K971831.

Who is the listed applicant for QUICK CHECK INSTANT THERMOMETER?

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

What is the FDA product code for QUICK CHECK INSTANT THERMOMETER?

The FDA product code for QUICK CHECK INSTANT 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.

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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