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FDA 510(k)

CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS

K-Number: K910020 · 1991-04-08

ApplicantCapintec Instruments, Inc.
Decision Date1991-04-08
Product CodeIZO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Capintec Instruments, Inc.. It received FDA 510(k) clearance on 1991-04-08 under 510(k) number K910020. The device is classified under product code IZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS?

CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1991-04-08. The listed applicant is Capintec Instruments, Inc.. The 510(k) number is K910020.

When did CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS receive FDA 510(k) clearance?

CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS received FDA 510(k) clearance on 1991-04-08, under 510(k) number K910020.

Who is the listed applicant for CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS?

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

What is the FDA product code for CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS?

The FDA product code for CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS is IZO.

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Other records listing Capintec 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.

K943072BETA C COUNTERK935539CAPINTEC CRC 35RK930962CAPTUS 2000 WEL COUNTERK924586CAPTUS 500 WELL DETECTOR W/CLINICAL LABOR SOFTWAREK921428CAPTUS 500K905796DOSE CALIBRATOR

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Related Devices (Code: IZO)

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.

K954666MPH50, MPH65, AND MPH80GE Medical SystemsK953582HFX350, 30KW, 300MA, 1 OR 3 PHASE RADIOGRAPHIC & FLUOROSCOPIC X-RAY GENERATORVarian Canada, Inc.K953831N 800 HFNucletron-Oldelft Corp.K952822SHIMADZU X-RAY HIGH VILTAGE GENERATOR AHD150GShimadzu Corp.K952265MILESTONW 350/450/550HF, PCX N350/450/550HF, TOP-X 350/450/550HF RADIOGRAPHIC X-RAY GENERATORControl-X, Inc.K950883POLYDOROS SX 65 AND 80Siemens Medical Solutions USA, Inc.

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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