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)

DISPOSINEEDLE SHARPS DISPOSAL UNIT

K-Number: K897095 · 1990-01-17

Decision Date1990-01-17
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSINEEDLE SHARPS DISPOSAL UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1990-01-17 under 510(k) number K897095. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSINEEDLE SHARPS DISPOSAL UNIT?

DISPOSINEEDLE SHARPS DISPOSAL UNIT is a medical device that received FDA 510(k) clearance on 1990-01-17. The listed applicant is Specialites Septodont. The 510(k) number is K897095.

When did DISPOSINEEDLE SHARPS DISPOSAL UNIT receive FDA 510(k) clearance?

DISPOSINEEDLE SHARPS DISPOSAL UNIT received FDA 510(k) clearance on 1990-01-17, under 510(k) number K897095.

Who is the listed applicant for DISPOSINEEDLE SHARPS DISPOSAL UNIT?

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

What is the FDA product code for DISPOSINEEDLE SHARPS DISPOSAL UNIT?

The FDA product code for DISPOSINEEDLE SHARPS DISPOSAL UNIT is MMK.

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 Specialites Septodont 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 21 devices →

Related Devices (Code: MMK)

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.

↑