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)

CONFORM ELASTIC NETTING

K-Number: K771563 · 1977-09-12

Decision Date1977-09-12
Product CodeFQM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CONFORM ELASTIC NETTING is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Research Center. It received FDA 510(k) clearance on 1977-09-12 under 510(k) number K771563. The device is classified under product code FQM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONFORM ELASTIC NETTING?

CONFORM ELASTIC NETTING is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Kendall Research Center. The 510(k) number is K771563.

When did CONFORM ELASTIC NETTING receive FDA 510(k) clearance?

CONFORM ELASTIC NETTING received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771563.

Who is the listed applicant for CONFORM ELASTIC NETTING?

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

What is the FDA product code for CONFORM ELASTIC NETTING?

The FDA product code for CONFORM ELASTIC NETTING is FQM.

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 Kendall Research Center 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 14 devices →

Related Devices (Code: FQM)

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.

↑