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FDA 510(k)

DR GREENBURGS HYBRID ACRYLIC

K-Number: K120371 · 2012-06-27

ApplicantAlways More Marketing, Inc.
Decision Date2012-06-27
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DR GREENBURGS HYBRID ACRYLIC is the device name listed in this FDA 510(k) record. The listed applicant is Always More Marketing, Inc.. It received FDA 510(k) clearance on 2012-06-27 under 510(k) number K120371. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR GREENBURGS HYBRID ACRYLIC?

DR GREENBURGS HYBRID ACRYLIC is a medical device that received FDA 510(k) clearance on 2012-06-27. The listed applicant is Always More Marketing, Inc.. The 510(k) number is K120371.

When did DR GREENBURGS HYBRID ACRYLIC receive FDA 510(k) clearance?

DR GREENBURGS HYBRID ACRYLIC received FDA 510(k) clearance on 2012-06-27, under 510(k) number K120371.

Who is the listed applicant for DR GREENBURGS HYBRID ACRYLIC?

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

What is the FDA product code for DR GREENBURGS HYBRID ACRYLIC?

The FDA product code for DR GREENBURGS HYBRID ACRYLIC is LRK.

Related Clinical Trials

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Other records listing Always More Marketing, 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.

K120372DR GREENBURGS HYBRID VACUUMK111680DR. GREENSBURG'S HYBRID

Related Devices (Code: LRK)

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.

K262104Anti Snoring Mouthpiece (L09-BB, L09-PP, L09-TB, L09-BT, L09-TP, L09-PT, L09-TT)Ram.Shaw Pte., Ltd.K261912SnØreNegatØrDnB Innovations, LLCK261366VirtusSomnomed, Inc.K261251Snorbliss® Anti-Snoring DeviceEndeavor Commerce, LLCK261134Dormiva Anti-Snoring Mouth GuardKoncept Innovators, Inc.K252942ShaeferHShaeferh, LLC

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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