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FDA 510(k)

CASANDRA SYRINGE CAP

K-Number: K871443 · 1987-08-18

Decision Date1987-08-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CASANDRA SYRINGE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Casandra Medical Corp.. It received FDA 510(k) clearance on 1987-08-18 under 510(k) number K871443. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CASANDRA SYRINGE CAP?

CASANDRA SYRINGE CAP is a medical device that received FDA 510(k) clearance on 1987-08-18. The listed applicant is Casandra Medical Corp.. The 510(k) number is K871443.

When did CASANDRA SYRINGE CAP receive FDA 510(k) clearance?

CASANDRA SYRINGE CAP received FDA 510(k) clearance on 1987-08-18, under 510(k) number K871443.

Who is the listed applicant for CASANDRA SYRINGE CAP?

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

What is the FDA product code for CASANDRA SYRINGE CAP?

The FDA product code for CASANDRA SYRINGE CAP is FMF.

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.

Related Devices (Code: FMF)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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