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)

OMED SILICONE LOOPS

K-Number: K810260 · 1981-02-26

Decision Date1981-02-26
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OMED SILICONE LOOPS is the device name listed in this FDA 510(k) record. The listed applicant is Omega-Med Intl., Inc.. It received FDA 510(k) clearance on 1981-02-26 under 510(k) number K810260. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OMED SILICONE LOOPS?

OMED SILICONE LOOPS is a medical device that received FDA 510(k) clearance on 1981-02-26. The listed applicant is Omega-Med Intl., Inc.. The 510(k) number is K810260.

When did OMED SILICONE LOOPS receive FDA 510(k) clearance?

OMED SILICONE LOOPS received FDA 510(k) clearance on 1981-02-26, under 510(k) number K810260.

Who is the listed applicant for OMED SILICONE LOOPS?

The FDA 510(k) record lists Omega-Med Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OMED SILICONE LOOPS?

The FDA product code for OMED SILICONE LOOPS is KDC.

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 Omega-Med Intl., 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 9 devices →

Related Devices (Code: KDC)

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.

↑