Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 a medical device manufactured by Microaire Surgical Instruments. It received FDA 510(k) clearance on 2020-05-14 under approval 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. It is manufactured by Microaire Surgical Instruments. The 510(k) number is K192694.

When was PAL Single-Use Cannulas approved by the FDA?

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

What company makes PAL Single-Use Cannulas?

PAL Single-Use Cannulas is manufactured by Microaire Surgical Instruments.

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

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

Other Devices by Microaire Surgical Instruments

Related Devices (Code: QPB)

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.