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FDA 510(k)

PADGETT SUCTION CANNULA

K-Number: K833717 · 1983-12-14

Decision Date1983-12-14
Product CodeGEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PADGETT SUCTION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Biosearch Assn.. It received FDA 510(k) clearance on 1983-12-14 under 510(k) number K833717. The device is classified under product code GEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PADGETT SUCTION CANNULA?

PADGETT SUCTION CANNULA is a medical device that received FDA 510(k) clearance on 1983-12-14. The listed applicant is Advanced Biosearch Assn.. The 510(k) number is K833717.

When did PADGETT SUCTION CANNULA receive FDA 510(k) clearance?

PADGETT SUCTION CANNULA received FDA 510(k) clearance on 1983-12-14, under 510(k) number K833717.

Who is the listed applicant for PADGETT SUCTION CANNULA?

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

What is the FDA product code for PADGETT SUCTION CANNULA?

The FDA product code for PADGETT SUCTION CANNULA is GEA.

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 Advanced Biosearch Assn. 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 22 devices →

Related Devices (Code: GEA)

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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