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

FDA 510(k)

WRIGHT DOW CORNING SOFTGOODS W/DOW

K-Number: K792269 · 1980-02-05

Decision Date1980-02-05
Product CodeIPY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

WRIGHT DOW CORNING SOFTGOODS W/DOW is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Wright. It received FDA 510(k) clearance on 1980-02-05 under 510(k) number K792269. The device is classified under product code IPY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WRIGHT DOW CORNING SOFTGOODS W/DOW?

WRIGHT DOW CORNING SOFTGOODS W/DOW is a medical device that received FDA 510(k) clearance on 1980-02-05. The listed applicant is Dow Corning Wright. The 510(k) number is K792269.

When did WRIGHT DOW CORNING SOFTGOODS W/DOW receive FDA 510(k) clearance?

WRIGHT DOW CORNING SOFTGOODS W/DOW received FDA 510(k) clearance on 1980-02-05, under 510(k) number K792269.

Who is the listed applicant for WRIGHT DOW CORNING SOFTGOODS W/DOW?

The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WRIGHT DOW CORNING SOFTGOODS W/DOW?

The FDA product code for WRIGHT DOW CORNING SOFTGOODS W/DOW is IPY.

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 Dow Corning Wright 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 74 devices →

Related Devices (Code: IPY)

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.

↑