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)

URINARY 17-KETOSTERIOD/17

K-Number: K772337 · 1978-01-12

ApplicantEppendorf-Brinkmann, Inc.
Decision Date1978-01-12
Product CodeCDG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

URINARY 17-KETOSTERIOD/17 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 1978-01-12 under 510(k) number K772337. The device is classified under product code CDG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY 17-KETOSTERIOD/17?

URINARY 17-KETOSTERIOD/17 is a medical device that received FDA 510(k) clearance on 1978-01-12. The listed applicant is Eppendorf-Brinkmann, Inc.. The 510(k) number is K772337.

When did URINARY 17-KETOSTERIOD/17 receive FDA 510(k) clearance?

URINARY 17-KETOSTERIOD/17 received FDA 510(k) clearance on 1978-01-12, under 510(k) number K772337.

Who is the listed applicant for URINARY 17-KETOSTERIOD/17?

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 URINARY 17-KETOSTERIOD/17?

The FDA product code for URINARY 17-KETOSTERIOD/17 is CDG.

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 KITK772151URINARY VMA - SCREEN TEST KITK761271URIN. L7-OH CORTICOSTEROID T(NON HYDRO)

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.

↑