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FDA 510(k)

INHAMATIC 33

K-Number: K781742 · 1978-12-04

ApplicantMedimatic
Decision Date1978-12-04
Product CodeIZD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INHAMATIC 33 is the device name listed in this FDA 510(k) record. The listed applicant is Medimatic. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781742. 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 INHAMATIC 33?

INHAMATIC 33 is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Medimatic. The 510(k) number is K781742.

When did INHAMATIC 33 receive FDA 510(k) clearance?

INHAMATIC 33 received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781742.

Who is the listed applicant for INHAMATIC 33?

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

What is the FDA product code for INHAMATIC 33?

The FDA product code for INHAMATIC 33 is IZD.

Related Clinical Trials

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Other records listing Medimatic 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.

K862511TOMOMATIC 232K851128DIGITMATIC DM2K810006TOMOMATIC 64K781352STRAIN GAUGE PLETHYSMOGRAPH

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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