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FDA 510(k)

PHARMASEED, MODEL BT-125-3

K-Number: K994018 · 2000-07-17

Decision Date2000-07-17
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHARMASEED, MODEL BT-125-3 is the device name listed in this FDA 510(k) record. The listed applicant is Syncor Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2000-07-17 under 510(k) number K994018. The device is classified under product code KXK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHARMASEED, MODEL BT-125-3?

PHARMASEED, MODEL BT-125-3 is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is Syncor Pharmaceuticals, Inc.. The 510(k) number is K994018.

When did PHARMASEED, MODEL BT-125-3 receive FDA 510(k) clearance?

PHARMASEED, MODEL BT-125-3 received FDA 510(k) clearance on 2000-07-17, under 510(k) number K994018.

Who is the listed applicant for PHARMASEED, MODEL BT-125-3?

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

What is the FDA product code for PHARMASEED, MODEL BT-125-3?

The FDA product code for PHARMASEED, MODEL BT-125-3 is KXK.

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 Syncor Pharmaceuticals, 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.

Related Devices (Code: KXK)

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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