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FDA 510(k)

ATS DOBELL & O'CONNOR'S IODINE

K-Number: K890861 · 1989-03-23

Decision Date1989-03-23
Product CodeJTS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ATS DOBELL & O'CONNOR'S IODINE is the device name listed in this FDA 510(k) record. The listed applicant is Alpha-Tec Systems, Inc.. It received FDA 510(k) clearance on 1989-03-23 under 510(k) number K890861. The device is classified under product code JTS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATS DOBELL & O'CONNOR'S IODINE?

ATS DOBELL & O'CONNOR'S IODINE is a medical device that received FDA 510(k) clearance on 1989-03-23. The listed applicant is Alpha-Tec Systems, Inc.. The 510(k) number is K890861.

When did ATS DOBELL & O'CONNOR'S IODINE receive FDA 510(k) clearance?

ATS DOBELL & O'CONNOR'S IODINE received FDA 510(k) clearance on 1989-03-23, under 510(k) number K890861.

Who is the listed applicant for ATS DOBELL & O'CONNOR'S IODINE?

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

What is the FDA product code for ATS DOBELL & O'CONNOR'S IODINE?

The FDA product code for ATS DOBELL & O'CONNOR'S IODINE is JTS.

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 Alpha-Tec 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 18 devices →

Related Devices (Code: JTS)

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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