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)

STERILE PROCEDURAL TRAYS

K-Number: K870373 · 1987-03-20

ApplicantDimed, Intl.
Decision Date1987-03-20
Product CodeKDD
Advisory CommitteeSU
DecisionUnknown

Device Summary

STERILE PROCEDURAL TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is Dimed, Intl.. It received FDA 510(k) clearance on 1987-03-20 under 510(k) number K870373. 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 STERILE PROCEDURAL TRAYS?

STERILE PROCEDURAL TRAYS is a medical device that received FDA 510(k) clearance on 1987-03-20. The listed applicant is Dimed, Intl.. The 510(k) number is K870373.

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

STERILE PROCEDURAL TRAYS received FDA 510(k) clearance on 1987-03-20, under 510(k) number K870373.

Who is the listed applicant for STERILE PROCEDURAL TRAYS?

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

What is the FDA product code for STERILE PROCEDURAL TRAYS?

The FDA product code for STERILE PROCEDURAL TRAYS 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 Dimed, Intl. 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.

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.

↑