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FDA 510(k)

FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)

K-Number: K900824 · 1990-05-22

ApplicantMidwest Orthodontic Mfg.
Decision Date1990-05-22
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Orthodontic Mfg.. It received FDA 510(k) clearance on 1990-05-22 under 510(k) number K900824. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)?

FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM) is a medical device that received FDA 510(k) clearance on 1990-05-22. The listed applicant is Midwest Orthodontic Mfg.. The 510(k) number is K900824.

When did FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM) receive FDA 510(k) clearance?

FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM) received FDA 510(k) clearance on 1990-05-22, under 510(k) number K900824.

Who is the listed applicant for FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)?

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

What is the FDA product code for FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)?

The FDA product code for FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM) is EJF.

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 Midwest Orthodontic Mfg. 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.

K981433ORTHODONTIC BRACESK955740GLUFLORMAK952856LIGHT-CURE PCK952855PC-LOCKK952858LIGHT-CUREK952857PRO-LOCK

View all 7 devices →

Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, 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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