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 GAUZE TRAYS

K-Number: K931759 · 1994-01-25

Decision Date1994-01-25
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

CARAPACE STERILE GAUZE TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Carapace, Inc.. It received FDA 510(k) clearance on 1994-01-25 under 510(k) number K931759. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CARAPACE STERILE GAUZE TRAYS?

CARAPACE STERILE GAUZE TRAYS is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Carapace, Inc.. The 510(k) number is K931759.

When did CARAPACE STERILE GAUZE TRAYS receive FDA 510(k) clearance?

CARAPACE STERILE GAUZE TRAYS received FDA 510(k) clearance on 1994-01-25, under 510(k) number K931759.

Who is the listed applicant for CARAPACE STERILE GAUZE TRAYS?

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 GAUZE TRAYS?

The FDA product code for CARAPACE STERILE GAUZE TRAYS is LRO.

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: LRO)

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.

↑