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)

E-CLIP

K-Number: K900982 · 1990-04-19

Decision Date1990-04-19
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E-CLIP is the device name listed in this FDA 510(k) record. The listed applicant is Joel Cohen & Esther R. Cohen. It received FDA 510(k) clearance on 1990-04-19 under 510(k) number K900982. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the E-CLIP?

E-CLIP is a medical device that received FDA 510(k) clearance on 1990-04-19. The listed applicant is Joel Cohen & Esther R. Cohen. The 510(k) number is K900982.

When did E-CLIP receive FDA 510(k) clearance?

E-CLIP received FDA 510(k) clearance on 1990-04-19, under 510(k) number K900982.

Who is the listed applicant for E-CLIP?

The FDA 510(k) record lists Joel Cohen & Esther R. Cohen as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-CLIP?

The FDA product code for E-CLIP is LDF.

Related Devices (Code: LDF)

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.

↑