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)

SPECIALTY SPONGES

K-Number: K781420 · 1978-10-03

ApplicantIpco Corp.
Decision Date1978-10-03
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

SPECIALTY SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Ipco Corp.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K781420. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIALTY SPONGES?

SPECIALTY SPONGES is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Ipco Corp.. The 510(k) number is K781420.

When did SPECIALTY SPONGES receive FDA 510(k) clearance?

SPECIALTY SPONGES received FDA 510(k) clearance on 1978-10-03, under 510(k) number K781420.

Who is the listed applicant for SPECIALTY SPONGES?

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

What is the FDA product code for SPECIALTY SPONGES?

The FDA product code for SPECIALTY SPONGES is EFQ.

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 Ipco Corp. 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 23 devices →

Related Devices (Code: EFQ)

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.

↑