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)

UNICATCH

K-Number: K770387 · 1977-04-05

ApplicantW.G. Whitney Corp.
Decision Date1977-04-05
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

UNICATCH is the device name listed in this FDA 510(k) record. The listed applicant is W.G. Whitney Corp.. It received FDA 510(k) clearance on 1977-04-05 under 510(k) number K770387. The device is classified under product code FMH. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNICATCH?

UNICATCH is a medical device that received FDA 510(k) clearance on 1977-04-05. The listed applicant is W.G. Whitney Corp.. The 510(k) number is K770387.

When did UNICATCH receive FDA 510(k) clearance?

UNICATCH received FDA 510(k) clearance on 1977-04-05, under 510(k) number K770387.

Who is the listed applicant for UNICATCH?

The FDA 510(k) record lists W.G. Whitney Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNICATCH?

The FDA product code for UNICATCH is FMH.

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 W.G. Whitney Corp. 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.

K834532STERILE WET DRESSING PACKK813535XEROFORM DRESSINGK810406STERILE WET DRESSING PACKK803299COLD/HOT PACKK800907TOMAC WET DRESSING WARMERK781322STERILE WET DRESSING PACK

View all 7 devices →

Related Devices (Code: FMH)

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.

K900983TRI-TECH URINE SPECIMEN KITTri-Tech, Inc.K823763VARIOUS-SPECIMEN COLLECTORSCordis Corp.K820180CALCULI FILTER CUPOmnimedicalK812933LANCER SPECIMEN CONTAINERSherwood Medical Co.K802340SPECIMEN SETAmerican Pharmaseal Div. AhscK802002URINE SPECIMEN CONTAINER #'S 1013-1016Pollak (Intl.), Ltd.

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.

↑