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FDA 510(k)

PHARMASEED, MODEL BT-125-2

K-Number: K993701 · 2000-06-09

ApplicantSyncor International, Inc.
Decision Date2000-06-09
Product CodeKXK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHARMASEED, MODEL BT-125-2 is the device name listed in this FDA 510(k) record. The listed applicant is Syncor International, Inc.. It received FDA 510(k) clearance on 2000-06-09 under 510(k) number K993701. 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-125-2?

PHARMASEED, MODEL BT-125-2 is a medical device that received FDA 510(k) clearance on 2000-06-09. The listed applicant is Syncor International, Inc.. The 510(k) number is K993701.

When did PHARMASEED, MODEL BT-125-2 receive FDA 510(k) clearance?

PHARMASEED, MODEL BT-125-2 received FDA 510(k) clearance on 2000-06-09, under 510(k) number K993701.

Who is the listed applicant for PHARMASEED, MODEL BT-125-2?

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

What is the FDA product code for PHARMASEED, MODEL BT-125-2?

The FDA product code for PHARMASEED, MODEL BT-125-2 is KXK.

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Other records listing Syncor International, 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.

K993700PHARMASEED, MODEL BT-103-2

Related Devices (Code: KXK)

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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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