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FDA 510(k)

TUBING SYRING

K-Number: K854699 · 1986-01-06

ApplicantAlmore Intl., Inc.
Decision Date1986-01-06
Product CodeECB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TUBING SYRING 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 1986-01-06 under 510(k) number K854699. The device is classified under product code ECB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING SYRING?

TUBING SYRING is a medical device that received FDA 510(k) clearance on 1986-01-06. The listed applicant is Almore Intl., Inc.. The 510(k) number is K854699.

When did TUBING SYRING receive FDA 510(k) clearance?

TUBING SYRING received FDA 510(k) clearance on 1986-01-06, under 510(k) number K854699.

Who is the listed applicant for TUBING SYRING?

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

What is the FDA product code for TUBING SYRING?

The FDA product code for TUBING SYRING is ECB.

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.

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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-HANDPIECEK854700EZ-ON TUBING CONDITIONER (LUBRICANT)

View all 21 devices →

Related Devices (Code: ECB)

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.

K942519UNI-SYRINGE, UNI-TIP AND ACCESS SYRINGE TIPSBull Frog Mfg. Co.K931772SURETIP SYRINGE TIP COVERWestern M/D, Inc.K931137DENTAL SYRINGE TIPA-Dec, Inc.K923876RISKONTROL SINGLE USERiskontrolK923285PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLESmith & Nephew, Inc.K920499SANI-TIPDw Industries, Inc.

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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