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FDA 510(k)

EZ-ON TUBING CONDITIONER (LUBRICANT)

K-Number: K854700 · 1986-03-12

ApplicantAlmore Intl., Inc.
Decision Date1986-03-12
Product Code
DecisionSubstantially Equivalent

Device Summary

EZ-ON TUBING CONDITIONER (LUBRICANT) is the device name listed in this FDA 510(k) record. The listed applicant is Almore Intl., Inc.. It received FDA 510(k) clearance on 1986-03-12 under 510(k) number K854700. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-ON TUBING CONDITIONER (LUBRICANT)?

EZ-ON TUBING CONDITIONER (LUBRICANT) is a medical device that received FDA 510(k) clearance on 1986-03-12. The listed applicant is Almore Intl., Inc.. The 510(k) number is K854700.

When did EZ-ON TUBING CONDITIONER (LUBRICANT) receive FDA 510(k) clearance?

EZ-ON TUBING CONDITIONER (LUBRICANT) received FDA 510(k) clearance on 1986-03-12, under 510(k) number K854700.

Who is the listed applicant for EZ-ON TUBING CONDITIONER (LUBRICANT)?

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

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Other records listing Almore Intl., Inc. 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.

K862851ALMORE FACE MASKK854692MONARCH II BLEACHING INSTRUMENTK854696OP II VISIBLE LIGHT CURING SYSTEMK854690DIAMONDS BURS-COMPOSIT FINISHINGK854691DIAMOND BURS-HANDPIECEK854701RETRACT-A-CORD

View all 21 devices →

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.

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