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FDA 510(k)

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE

K-Number: K827748 · 1982-08-16

ApplicantKemble Instruments, Inc.
Decision Date1982-08-16
Product Code
DecisionSubstantially Equivalent

Device Summary

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Kemble Instruments, Inc.. It received FDA 510(k) clearance on 1982-08-16 under 510(k) number K827748. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE?

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Kemble Instruments, Inc.. The 510(k) number is K827748.

When did THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE receive FDA 510(k) clearance?

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE received FDA 510(k) clearance on 1982-08-16, under 510(k) number K827748.

Who is the listed applicant for THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE?

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

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Other records listing Kemble Instruments, 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.

K842894KEMBLE 405K832734KEMTEK 400 RIA GAMMA COUNTERK832760RIA SOFTWAREK832735KEMTEK 103 RIA GAMMA COUNTERK832736KEMTEK 104 RIA GAMMA COUNTERK830751KEMTEK 102

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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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