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)

DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS

K-Number: K915067 · 1992-03-11

Decision Date1992-03-11
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Corp.. It received FDA 510(k) clearance on 1992-03-11 under 510(k) number K915067. 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 DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS?

DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS is a medical device that received FDA 510(k) clearance on 1992-03-11. The listed applicant is American Medical Corp.. The 510(k) number is K915067.

When did DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS receive FDA 510(k) clearance?

DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS received FDA 510(k) clearance on 1992-03-11, under 510(k) number K915067.

Who is the listed applicant for DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS?

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

What is the FDA product code for DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS?

The FDA product code for DISPOSABLE NEEDLE COUNTERS & DISPOSABLE SYSTEMS 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 American Medical Corp. 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: 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.

↑