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FDA 510(k)

VAN DELLEN ASPIRATING TUBING

K-Number: K873463 · 1987-11-23

Decision Date1987-11-23
Product CodeBYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAN DELLEN ASPIRATING TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Van Dellen, Ltd.. It received FDA 510(k) clearance on 1987-11-23 under 510(k) number K873463. The device is classified under product code BYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAN DELLEN ASPIRATING TUBING?

VAN DELLEN ASPIRATING TUBING is a medical device that received FDA 510(k) clearance on 1987-11-23. The listed applicant is Van Dellen, Ltd.. The 510(k) number is K873463.

When did VAN DELLEN ASPIRATING TUBING receive FDA 510(k) clearance?

VAN DELLEN ASPIRATING TUBING received FDA 510(k) clearance on 1987-11-23, under 510(k) number K873463.

Who is the listed applicant for VAN DELLEN ASPIRATING TUBING?

The FDA 510(k) record lists Van Dellen, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAN DELLEN ASPIRATING TUBING?

The FDA product code for VAN DELLEN ASPIRATING TUBING is BYY.

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 Van Dellen, Ltd. 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 7 devices →

Related Devices (Code: BYY)

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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