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)

HANCOCK * OBTURATORS

K-Number: K801885 · 1980-09-09

ApplicantHancock Laboratories, Inc.
Decision Date1980-09-09
Product CodeDTI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HANCOCK * OBTURATORS 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 1980-09-09 under 510(k) number K801885. The device is classified under product code DTI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANCOCK * OBTURATORS?

HANCOCK * OBTURATORS is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Hancock Laboratories, Inc.. The 510(k) number is K801885.

When did HANCOCK * OBTURATORS receive FDA 510(k) clearance?

HANCOCK * OBTURATORS received FDA 510(k) clearance on 1980-09-09, under 510(k) number K801885.

Who is the listed applicant for HANCOCK * OBTURATORS?

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

What is the FDA product code for HANCOCK * OBTURATORS?

The FDA product code for HANCOCK * OBTURATORS is DTI.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hancock Laboratories, 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.

K800703MODIFIED CATHETER PACKAGEK800122HANCOCK AORTIC PUNCHK790534MERSILENE SUTURESK780568DURAN FLEXIBLE RING

Related Devices (Code: DTI)

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.

K952184CARBOMEDICS SUPRA-ANNULAR VALVE SIZERCarbomedics, Inc.K934951VALVE SIZERCarbomedics, Inc.K881279EDWARDS-DUROMEDICS BILEAFLET VALVE SIZER SETBaxter Healthcare CorpK853313DUROMEDICS CARDIAC VALVE SIZER SETHemex Scientific, Inc.K852612METRONIC MODEL F7700 HEART VALVE SIZERSMedtronic VascularK820887MITRAL VALVE ORIFICE SIZERCeltech

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.

↑