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)

LAPAROTOMY SPONGES

K-Number: K874065 · 1987-11-04

Decision Date1987-11-04
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

LAPAROTOMY SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Interpro Intl., Inc.. It received FDA 510(k) clearance on 1987-11-04 under 510(k) number K874065. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROTOMY SPONGES?

LAPAROTOMY SPONGES is a medical device that received FDA 510(k) clearance on 1987-11-04. The listed applicant is Interpro Intl., Inc.. The 510(k) number is K874065.

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

LAPAROTOMY SPONGES received FDA 510(k) clearance on 1987-11-04, under 510(k) number K874065.

Who is the listed applicant for LAPAROTOMY SPONGES?

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

What is the FDA product code for LAPAROTOMY SPONGES?

The FDA product code for LAPAROTOMY 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 Interpro 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 11 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.

↑