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FDA 510(k)

PAL Single-Use Cannulas

K-Number: K192694 · 2020-05-14

Decision Date2020-05-14
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PAL Single-Use Cannulas is the device name listed in this FDA 510(k) record. The listed applicant is Microaire Surgical Instruments. It received FDA 510(k) clearance on 2020-05-14 under 510(k) number K192694. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAL Single-Use Cannulas?

PAL Single-Use Cannulas is a medical device that received FDA 510(k) clearance on 2020-05-14. The listed applicant is Microaire Surgical Instruments. The 510(k) number is K192694.

When did PAL Single-Use Cannulas receive FDA 510(k) clearance?

PAL Single-Use Cannulas received FDA 510(k) clearance on 2020-05-14, under 510(k) number K192694.

Who is the listed applicant for PAL Single-Use Cannulas?

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

What is the FDA product code for PAL Single-Use Cannulas?

The FDA product code for PAL Single-Use Cannulas is QPB.

Other records listing Microaire Surgical Instruments 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 10 devices →

Related Devices (Code: QPB)

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.