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)

HYSTERECTOMY T DRAIN

K-Number: K782027 · 1978-12-20

ApplicantDavol, Inc.
Decision Date1978-12-20
Product CodeJOL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYSTERECTOMY T DRAIN is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K782027. The device is classified under product code JOL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYSTERECTOMY T DRAIN?

HYSTERECTOMY T DRAIN is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Davol, Inc.. The 510(k) number is K782027.

When did HYSTERECTOMY T DRAIN receive FDA 510(k) clearance?

HYSTERECTOMY T DRAIN received FDA 510(k) clearance on 1978-12-20, under 510(k) number K782027.

Who is the listed applicant for HYSTERECTOMY T DRAIN?

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

What is the FDA product code for HYSTERECTOMY T DRAIN?

The FDA product code for HYSTERECTOMY T DRAIN is JOL.

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 Davol, Inc. 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 50 devices →

Related Devices (Code: JOL)

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.

↑