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)

MODIFIED CHORIO-SHURE

K-Number: K832892 · 1983-10-28

Decision Date1983-10-28
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MODIFIED CHORIO-SHURE is the device name listed in this FDA 510(k) record. The listed applicant is Nuclear Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1983-10-28 under 510(k) number K832892. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED CHORIO-SHURE?

MODIFIED CHORIO-SHURE is a medical device that received FDA 510(k) clearance on 1983-10-28. The listed applicant is Nuclear Medical Laboratories, Inc.. The 510(k) number is K832892.

When did MODIFIED CHORIO-SHURE receive FDA 510(k) clearance?

MODIFIED CHORIO-SHURE received FDA 510(k) clearance on 1983-10-28, under 510(k) number K832892.

Who is the listed applicant for MODIFIED CHORIO-SHURE?

The FDA 510(k) record lists Nuclear Medical Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED CHORIO-SHURE?

The FDA product code for MODIFIED CHORIO-SHURE is JHI.

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.

Other records listing Nuclear Medical Laboratories, 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.

View all 24 devices →

Related Devices (Code: JHI)

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.

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.

↑