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FDA 510(k)

ACKRAD SIALOGRAPHY CATHETER

K-Number: K852154 · 1985-06-26

Decision Date1985-06-26
Product Code
DecisionSubstantially Equivalent

Device Summary

ACKRAD SIALOGRAPHY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Ackrad Laboratories. It received FDA 510(k) clearance on 1985-06-26 under 510(k) number K852154. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACKRAD SIALOGRAPHY CATHETER?

ACKRAD SIALOGRAPHY CATHETER is a medical device that received FDA 510(k) clearance on 1985-06-26. The listed applicant is Ackrad Laboratories. The 510(k) number is K852154.

When did ACKRAD SIALOGRAPHY CATHETER receive FDA 510(k) clearance?

ACKRAD SIALOGRAPHY CATHETER received FDA 510(k) clearance on 1985-06-26, under 510(k) number K852154.

Who is the listed applicant for ACKRAD SIALOGRAPHY CATHETER?

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

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 Ackrad Laboratories 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.

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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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