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)

URIN. L7-OH CORTICOSTEROID T(NON HYDRO)

K-Number: K761271 · 1977-02-14

ApplicantEppendorf-Brinkmann, Inc.
Decision Date1977-02-14
Product CodeCDB
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URIN. L7-OH CORTICOSTEROID T(NON HYDRO) is the device name listed in this FDA 510(k) record. The listed applicant is Eppendorf-Brinkmann, Inc.. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K761271. The device is classified under product code CDB. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URIN. L7-OH CORTICOSTEROID T(NON HYDRO)?

URIN. L7-OH CORTICOSTEROID T(NON HYDRO) is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is Eppendorf-Brinkmann, Inc.. The 510(k) number is K761271.

When did URIN. L7-OH CORTICOSTEROID T(NON HYDRO) receive FDA 510(k) clearance?

URIN. L7-OH CORTICOSTEROID T(NON HYDRO) received FDA 510(k) clearance on 1977-02-14, under 510(k) number K761271.

Who is the listed applicant for URIN. L7-OH CORTICOSTEROID T(NON HYDRO)?

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

What is the FDA product code for URIN. L7-OH CORTICOSTEROID T(NON HYDRO)?

The FDA product code for URIN. L7-OH CORTICOSTEROID T(NON HYDRO) is CDB.

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 Eppendorf-Brinkmann, 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.

K780819GLYCOHEMOGLOBIN-SKREEN TEST KITK772337URINARY 17-KETOSTERIOD/17K772151URINARY VMA - SCREEN TEST KIT

Related Devices (Code: CDB)

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.

K77242617-HYDROXY TESTHycel, Inc.

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.

↑