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)

INTER-PAL C-19 AND INTER-PAL C-38

K-Number: K890294 · 1990-02-01

ApplicantEnrad Corp.
Decision Date1990-02-01
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTER-PAL C-19 AND INTER-PAL C-38 is the device name listed in this FDA 510(k) record. The listed applicant is Enrad Corp.. It received FDA 510(k) clearance on 1990-02-01 under 510(k) number K890294. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTER-PAL C-19 AND INTER-PAL C-38?

INTER-PAL C-19 AND INTER-PAL C-38 is a medical device that received FDA 510(k) clearance on 1990-02-01. The listed applicant is Enrad Corp.. The 510(k) number is K890294.

When did INTER-PAL C-19 AND INTER-PAL C-38 receive FDA 510(k) clearance?

INTER-PAL C-19 AND INTER-PAL C-38 received FDA 510(k) clearance on 1990-02-01, under 510(k) number K890294.

Who is the listed applicant for INTER-PAL C-19 AND INTER-PAL C-38?

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

What is the FDA product code for INTER-PAL C-19 AND INTER-PAL C-38?

The FDA product code for INTER-PAL C-19 AND INTER-PAL C-38 is JAQ.

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

Related Devices (Code: JAQ)

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.

K262383LumenCare AzureNucletron B.V.K252717MAASTRO Rectal Applicator SetVarian Medical SystemsK251037Rectal ApplicatorNucletron B.V.K252884Guided Aarhus Applicator SetVarian Medical SystemsK250299CT/ MR Tandem and Ovoid SetVarian Medical Systems, Inc.K250289Intracavitary/Interstitial SystemVarian Medical Systems

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.

↑