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)

TAMPER PROOF CAP

K-Number: K861276 · 1986-05-05

Decision Date1986-05-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TAMPER PROOF CAP is the device name listed in this FDA 510(k) record. The listed applicant is Intl. Medical Industries. It received FDA 510(k) clearance on 1986-05-05 under 510(k) number K861276. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPER PROOF CAP?

TAMPER PROOF CAP is a medical device that received FDA 510(k) clearance on 1986-05-05. The listed applicant is Intl. Medical Industries. The 510(k) number is K861276.

When did TAMPER PROOF CAP receive FDA 510(k) clearance?

TAMPER PROOF CAP received FDA 510(k) clearance on 1986-05-05, under 510(k) number K861276.

Who is the listed applicant for TAMPER PROOF CAP?

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

What is the FDA product code for TAMPER PROOF CAP?

The FDA product code for TAMPER PROOF CAP is FMF.

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 Intl. Medical Industries 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: FMF)

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.

↑