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)

CARAPACE STERILE COTTON BALLS

K-Number: K931626 · 1993-12-02

Decision Date1993-12-02
Product CodeFRL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CARAPACE STERILE COTTON BALLS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1993-12-02 under 510(k) number K931626. The device is classified under product code FRL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARAPACE STERILE COTTON BALLS?

CARAPACE STERILE COTTON BALLS is a medical device that received FDA 510(k) clearance on 1993-12-02. The listed applicant is Carapace, Inc.. The 510(k) number is K931626.

When did CARAPACE STERILE COTTON BALLS receive FDA 510(k) clearance?

CARAPACE STERILE COTTON BALLS received FDA 510(k) clearance on 1993-12-02, under 510(k) number K931626.

Who is the listed applicant for CARAPACE STERILE COTTON BALLS?

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

What is the FDA product code for CARAPACE STERILE COTTON BALLS?

The FDA product code for CARAPACE STERILE COTTON BALLS is FRL.

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 Carapace, 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 22 devices →

Related Devices (Code: FRL)

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.

↑