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)

DEXIDE LAPAROSCOPIC KITS

K-Number: K924117 · 1993-03-23

ApplicantDexide, Inc.
Decision Date1993-03-23
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

DEXIDE LAPAROSCOPIC KITS is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1993-03-23 under 510(k) number K924117. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DEXIDE LAPAROSCOPIC KITS?

DEXIDE LAPAROSCOPIC KITS is a medical device that received FDA 510(k) clearance on 1993-03-23. The listed applicant is Dexide, Inc.. The 510(k) number is K924117.

When did DEXIDE LAPAROSCOPIC KITS receive FDA 510(k) clearance?

DEXIDE LAPAROSCOPIC KITS received FDA 510(k) clearance on 1993-03-23, under 510(k) number K924117.

Who is the listed applicant for DEXIDE LAPAROSCOPIC KITS?

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

What is the FDA product code for DEXIDE LAPAROSCOPIC KITS?

The FDA product code for DEXIDE LAPAROSCOPIC KITS is KDD.

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 Dexide, 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 38 devices →

Related Devices (Code: KDD)

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.

↑