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FDA 510(k)

THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900

K-Number: K913055 · 1991-09-06

ApplicantAtomic Products Corp.
Decision Date1991-09-06
Product CodeIZD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 is the device name listed in this FDA 510(k) record. The listed applicant is Atomic Products Corp.. It received FDA 510(k) clearance on 1991-09-06 under 510(k) number K913055. The device is classified under product code IZD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900?

THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 is a medical device that received FDA 510(k) clearance on 1991-09-06. The listed applicant is Atomic Products Corp.. The 510(k) number is K913055.

When did THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 receive FDA 510(k) clearance?

THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 received FDA 510(k) clearance on 1991-09-06, under 510(k) number K913055.

Who is the listed applicant for THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900?

The FDA 510(k) record lists Atomic Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900?

The FDA product code for THYROID UPTAKE SYST/AUTOMLAB 900 MEDI SPEC 187-900 is IZD.

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Other records listing Atomic Products Corp. 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.

K915541SPECT TABLE, MODEL #056-760K904187ECONOMY C-ARM TABLE, MODEL # 056-005K904623RADIOGRAPHIC TRANSPORT, TRAUMA MODEL 056-230, 235K900851DIGITAL IMAGE ENHANCEMENT SYSTEMK895799RECTILINEAR SCANNER MODEL #187-270K884312ATOMLAB 100, MODEL 086-250 & 200 MODEL 086-270

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Related Devices (Code: IZD)

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.

K123917DECLIPSESPECT VIEWERSurgiceye GmbHK101887CONFIDENT SURGERY SUITE 300, MODEL CSS300Surgiceye GmbHK013751HANDHELD GAMMA FINDER (HGF)Silicon Instruments GmhbK983768MODIFICATION TO GAMMA GUIDANCE SYSTEMRadiation Monitoring Devices, Inc.K982442C-TRAK AUTOMATIC ANALYZER (NAME CHANGE FROM ONCOPROBE II TO C-TRAK)Care Wise Medical Products Corp.K971167NEOPROBE MODEL 1500 PORTABLE RADIOISOTOPE DETECTOR AND ACCESSORIESNeoprobe Corp.

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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