FDA 510(k)

DURAN FLEXIBLE RING

K-Number: K780568 · 1978-05-26

Decision Date1978-05-26

Product Code

DecisionSubstantially Equivalent

Device Summary

DURAN FLEXIBLE RING is the device name listed in this FDA 510(k) record. The listed applicant is Hancock Laboratories, Inc.. It received FDA 510(k) clearance on 1978-05-26 under 510(k) number K780568. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURAN FLEXIBLE RING?

DURAN FLEXIBLE RING is a medical device that received FDA 510(k) clearance on 1978-05-26. The listed applicant is Hancock Laboratories, Inc.. The 510(k) number is K780568.

When did DURAN FLEXIBLE RING receive FDA 510(k) clearance?

DURAN FLEXIBLE RING received FDA 510(k) clearance on 1978-05-26, under 510(k) number K780568.

Who is the listed applicant for DURAN FLEXIBLE RING?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hancock Laboratories, Inc. as applicant

K801885HANCOCK * OBTURATORS K800703MODIFIED CATHETER PACKAGE K800122HANCOCK AORTIC PUNCH K790534MERSILENE SUTURES

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.