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FDA 510(k)

TWO TANK DISSOLUTION MODULE

K-Number: K893612 · 1989-07-24

Decision Date1989-07-24
Product CodeFKQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TWO TANK DISSOLUTION MODULE is the device name listed in this FDA 510(k) record. The listed applicant is National Medical Care, Medical Products Div., Inc.. It received FDA 510(k) clearance on 1989-07-24 under 510(k) number K893612. The device is classified under product code FKQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TWO TANK DISSOLUTION MODULE?

TWO TANK DISSOLUTION MODULE is a medical device that received FDA 510(k) clearance on 1989-07-24. The listed applicant is National Medical Care, Medical Products Div., Inc.. The 510(k) number is K893612.

When did TWO TANK DISSOLUTION MODULE receive FDA 510(k) clearance?

TWO TANK DISSOLUTION MODULE received FDA 510(k) clearance on 1989-07-24, under 510(k) number K893612.

Who is the listed applicant for TWO TANK DISSOLUTION MODULE?

The FDA 510(k) record lists National Medical Care, Medical Products Div., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWO TANK DISSOLUTION MODULE?

The FDA product code for TWO TANK DISSOLUTION MODULE is FKQ.

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 National Medical Care, Medical Products Div., 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 62 devices →

Related Devices (Code: FKQ)

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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