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FDA 510(k)

CM-II, CM-I WATER UNIT

K-Number: K863021 · 1986-10-01

Decision Date1986-10-01
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CM-II, CM-I WATER UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Sds Dental, Inc.. It received FDA 510(k) clearance on 1986-10-01 under 510(k) number K863021. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CM-II, CM-I WATER UNIT?

CM-II, CM-I WATER UNIT is a medical device that received FDA 510(k) clearance on 1986-10-01. The listed applicant is Sds Dental, Inc.. The 510(k) number is K863021.

When did CM-II, CM-I WATER UNIT receive FDA 510(k) clearance?

CM-II, CM-I WATER UNIT received FDA 510(k) clearance on 1986-10-01, under 510(k) number K863021.

Who is the listed applicant for CM-II, CM-I WATER UNIT?

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

What is the FDA product code for CM-II, CM-I WATER UNIT?

The FDA product code for CM-II, CM-I WATER UNIT is EIA.

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 Sds Dental, 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 21 devices →

Related Devices (Code: EIA)

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

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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