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)

SUTURE SET OR LACERATION TRAYS (PACKS)

K-Number: K932219 · 1993-07-09

Decision Date1993-07-09
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

SUTURE SET OR LACERATION TRAYS (PACKS) is the device name listed in this FDA 510(k) record. The listed applicant is Associated Medical Products Co.. It received FDA 510(k) clearance on 1993-07-09 under 510(k) number K932219. 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 SUTURE SET OR LACERATION TRAYS (PACKS)?

SUTURE SET OR LACERATION TRAYS (PACKS) is a medical device that received FDA 510(k) clearance on 1993-07-09. The listed applicant is Associated Medical Products Co.. The 510(k) number is K932219.

When did SUTURE SET OR LACERATION TRAYS (PACKS) receive FDA 510(k) clearance?

SUTURE SET OR LACERATION TRAYS (PACKS) received FDA 510(k) clearance on 1993-07-09, under 510(k) number K932219.

Who is the listed applicant for SUTURE SET OR LACERATION TRAYS (PACKS)?

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

What is the FDA product code for SUTURE SET OR LACERATION TRAYS (PACKS)?

The FDA product code for SUTURE SET OR LACERATION TRAYS (PACKS) 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 Associated Medical Products Co. 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 29 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.

↑