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FDA 510(k)

HASSON STABILIZING ACCESS CANNULA

K-Number: K903078 · 1990-12-17

Decision Date1990-12-17
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

HASSON STABILIZING ACCESS CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Marlo Surgical Technology. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K903078. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HASSON STABILIZING ACCESS CANNULA?

HASSON STABILIZING ACCESS CANNULA is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Marlo Surgical Technology. The 510(k) number is K903078.

When did HASSON STABILIZING ACCESS CANNULA receive FDA 510(k) clearance?

HASSON STABILIZING ACCESS CANNULA received FDA 510(k) clearance on 1990-12-17, under 510(k) number K903078.

Who is the listed applicant for HASSON STABILIZING ACCESS CANNULA?

The FDA 510(k) record lists Marlo Surgical Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HASSON STABILIZING ACCESS CANNULA?

The FDA product code for HASSON STABILIZING ACCESS CANNULA 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 Marlo Surgical Technology 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 28 devices →

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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