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FDA 510(k)

DISPOSABLE SYRINGE FILL TUBE

K-Number: K781334 · 1978-08-17

Decision Date1978-08-17
Product CodeDXT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SYRINGE FILL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Group, Inc.. It received FDA 510(k) clearance on 1978-08-17 under 510(k) number K781334. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SYRINGE FILL TUBE?

DISPOSABLE SYRINGE FILL TUBE is a medical device that received FDA 510(k) clearance on 1978-08-17. The listed applicant is Mallinckrodt Group, Inc.. The 510(k) number is K781334.

When did DISPOSABLE SYRINGE FILL TUBE receive FDA 510(k) clearance?

DISPOSABLE SYRINGE FILL TUBE received FDA 510(k) clearance on 1978-08-17, under 510(k) number K781334.

Who is the listed applicant for DISPOSABLE SYRINGE FILL TUBE?

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

What is the FDA product code for DISPOSABLE SYRINGE FILL TUBE?

The FDA product code for DISPOSABLE SYRINGE FILL TUBE is DXT.

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 Mallinckrodt Group, 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 27 devices →

Related Devices (Code: DXT)

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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