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FDA 510(k)

PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER

K-Number: K894286 · 1989-10-12

ApplicantPpg Industries, Inc.
Decision Date1989-10-12
Product CodeDXO
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Ppg Industries, Inc.. It received FDA 510(k) clearance on 1989-10-12 under 510(k) number K894286. The device is classified under product code DXO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER?

PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER is a medical device that received FDA 510(k) clearance on 1989-10-12. The listed applicant is Ppg Industries, Inc.. The 510(k) number is K894286.

When did PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER receive FDA 510(k) clearance?

PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER received FDA 510(k) clearance on 1989-10-12, under 510(k) number K894286.

Who is the listed applicant for PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER?

The FDA 510(k) record lists Ppg Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER?

The FDA product code for PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER is DXO.

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Other records listing Ppg Industries, Inc. as applicant

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Related Devices (Code: DXO)

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.

K251367OptoMonitor 3Opsens, Inc.K241418OptoMonitor 3Opsens, Inc.K233904ACIST RXi System (016616); ACIST Navvus II Catheter (016675_Acist Medical Systems, Inc.K222216TruWave Disposable Pressure TransducerEdwards Lifesciences, LLCK202943OptoMonitor 3Opsens, Inc.K193620OptoMonitor 3Opsens, Inc.

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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