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FDA 510(k)

DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555

K-Number: K904850 · 1991-01-25

ApplicantMicro Motors, Inc.
Decision Date1991-01-25
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Motors, Inc.. It received FDA 510(k) clearance on 1991-01-25 under 510(k) number K904850. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555?

DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 is a medical device that received FDA 510(k) clearance on 1991-01-25. The listed applicant is Micro Motors, Inc.. The 510(k) number is K904850.

When did DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 receive FDA 510(k) clearance?

DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 received FDA 510(k) clearance on 1991-01-25, under 510(k) number K904850.

Who is the listed applicant for DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555?

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

What is the FDA product code for DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555?

The FDA product code for DUAL AND SINGLE IRR. SYSTEMS MODELS 29550 & 29555 is EFS.

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Other records listing Micro Motors, 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.

K000120PRO-TORQK991283DYNA TORQ TORQUE WRENCH, TORQUE WRENCHK963843ELECTRIC SURGICAL IRRIGATION SYSTEM - DUAL CONTROLLER UNITK970002STERILE WATER PUMPK942380MICRO ICS SONIC SCALERK935676MICRO RSH HIGH SPEED HANDPIECE

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Related Devices (Code: EFS)

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.

K023232SPLATRFREE SWANGLE 360 DISPOSABLE PROPHYLAXIS ANGLESmartpracticeK001493DENTAL AIR FORCE HOME DENTAL CLEANING SYSTEM, MODEL NO. 0020001Air Force, Inc.K983374AGATHA-A-H2010Midian Intl.K964810DERMADAMUltradent Products, Inc.K952234BARRIER ALL FILMCottrell, Ltd.K943182ORAL-B PERIOFLEX SUBGINGIVAL IRRIGATOROral-B Laboratories

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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