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FDA 510(k)

CONPHAR DIGITAL THERMOMETER

K-Number: K813306 · 1982-01-28

ApplicantConphar, Inc.
Decision Date1982-01-28
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONPHAR DIGITAL THERMOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Conphar, Inc.. It received FDA 510(k) clearance on 1982-01-28 under 510(k) number K813306. 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 CONPHAR DIGITAL THERMOMETER?

CONPHAR DIGITAL THERMOMETER is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is Conphar, Inc.. The 510(k) number is K813306.

When did CONPHAR DIGITAL THERMOMETER receive FDA 510(k) clearance?

CONPHAR DIGITAL THERMOMETER received FDA 510(k) clearance on 1982-01-28, under 510(k) number K813306.

Who is the listed applicant for CONPHAR DIGITAL THERMOMETER?

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

What is the FDA product code for CONPHAR DIGITAL THERMOMETER?

The FDA product code for CONPHAR DIGITAL 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 Conphar, Inc. 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.

View all 122 devices →

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

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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