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)

BCD-HPP41C INTERFACE

K-Number: K810968 · 1981-04-23

ApplicantDynatech Corp.
Decision Date1981-04-23
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BCD-HPP41C INTERFACE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Corp.. It received FDA 510(k) clearance on 1981-04-23 under 510(k) number K810968. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BCD-HPP41C INTERFACE?

BCD-HPP41C INTERFACE is a medical device that received FDA 510(k) clearance on 1981-04-23. The listed applicant is Dynatech Corp.. The 510(k) number is K810968.

When did BCD-HPP41C INTERFACE receive FDA 510(k) clearance?

BCD-HPP41C INTERFACE received FDA 510(k) clearance on 1981-04-23, under 510(k) number K810968.

Who is the listed applicant for BCD-HPP41C INTERFACE?

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

What is the FDA product code for BCD-HPP41C INTERFACE?

The FDA product code for BCD-HPP41C INTERFACE is JQP.

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 Dynatech 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.

K904567DYNATECH MR4000 MICROPLATE READERK854603MULTI MASH 2000K854602MINI MASH 2000K854604AUTO MASHK832117IMMULON SUBSTRATE REMOVAWELL STRIPSK823787HANDI-WASH

View all 27 devices →

Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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.

↑