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FDA 510(k)

MIDAS 6000 AUTOMATIC STAINER

K-Number: K832994 · 1983-09-29

Decision Date1983-09-29
Product CodeKPA
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MIDAS 6000 AUTOMATIC STAINER is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Systems, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832994. The device is classified under product code KPA. It was reviewed by the PA advisory panel. Product code KPA falls under the category of Cardiovascular, which encompasses devices for cardiovascular diagnosis, monitoring, and intervention. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDAS 6000 AUTOMATIC STAINER?

MIDAS 6000 AUTOMATIC STAINER is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Innovative Medical Systems, Inc.. The 510(k) number is K832994.

When did MIDAS 6000 AUTOMATIC STAINER receive FDA 510(k) clearance?

MIDAS 6000 AUTOMATIC STAINER received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832994.

Who is the listed applicant for MIDAS 6000 AUTOMATIC STAINER?

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

What is the FDA product code for MIDAS 6000 AUTOMATIC STAINER?

The FDA product code for MIDAS 6000 AUTOMATIC STAINER is KPA. This falls under the Cardiovascular category.

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 Innovative Medical Systems, 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 22 devices →

Related Devices (Code: KPA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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