FDA 510(k)

TRANSFERSCREEN II

K-Number: K843857 · 1984-11-08

Decision Date1984-11-08

Product Code

DecisionSubstantially Equivalent

Device Summary

TRANSFERSCREEN II is the device name listed in this FDA 510(k) record. The listed applicant is Erich Jaeger, Inc.. It received FDA 510(k) clearance on 1984-11-08 under 510(k) number K843857. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSFERSCREEN II?

TRANSFERSCREEN II is a medical device that received FDA 510(k) clearance on 1984-11-08. The listed applicant is Erich Jaeger, Inc.. The 510(k) number is K843857.

When did TRANSFERSCREEN II receive FDA 510(k) clearance?

TRANSFERSCREEN II received FDA 510(k) clearance on 1984-11-08, under 510(k) number K843857.

Who is the listed applicant for TRANSFERSCREEN II?

The FDA 510(k) record lists Erich Jaeger, 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 Erich Jaeger, Inc. as applicant

K000396APNOESCREEN PRO, ALPHA SCREEN PRO K972419TOENNIES NEUROSCREEN SYSTEM K960078ASTHMA MONITOR K933839MASTER SCREEN PNUEMO K932744FLOWSCREEN K853443ALVEO-DIFFUSION TEST

View all 28 devices →

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.