HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM)
K-Number: K904645 · 1991-02-26
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Device Summary
Frequently Asked Questions
What is the HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM)?
HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM) is a medical device that received FDA 510(k) clearance on 1991-02-26. The listed applicant is Hall Medical Laboratories. The 510(k) number is K904645.
When did HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM) receive FDA 510(k) clearance?
HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM) received FDA 510(k) clearance on 1991-02-26, under 510(k) number K904645.
Who is the listed applicant for HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM)?
The FDA 510(k) record lists Hall Medical Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM)?
The FDA product code for HALL TRANSCEERVICAL SAFE ACCESS CANNULA(TM) is HET.
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 Hall Medical 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.
Related Devices (Code: HET)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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