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FDA 510(k)

DR. GREENSBURG'S HYBRID

K-Number: K111680 · 2011-12-23

ApplicantAlways More Marketing, Inc.
Decision Date2011-12-23
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DR. GREENSBURG'S HYBRID 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 2011-12-23 under 510(k) number K111680. 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. GREENSBURG'S HYBRID?

DR. GREENSBURG'S HYBRID is a medical device that received FDA 510(k) clearance on 2011-12-23. The listed applicant is Always More Marketing, Inc.. The 510(k) number is K111680.

When did DR. GREENSBURG'S HYBRID receive FDA 510(k) clearance?

DR. GREENSBURG'S HYBRID received FDA 510(k) clearance on 2011-12-23, under 510(k) number K111680.

Who is the listed applicant for DR. GREENSBURG'S HYBRID?

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. GREENSBURG'S HYBRID?

The FDA product code for DR. GREENSBURG'S HYBRID is LRK.

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 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 VACUUMK120371DR GREENBURGS HYBRID ACRYLIC

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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