Anesthesiology
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- MiscellaneousMiscellaneous
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart D—Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—General Hospital and Personal Use Therapeutic DevicesCFR Sub-Part
- NUPCream, Nasal, Topical, Mechanical Allergen Particle Barrier2Product Code
- K213114BentrioTM Allergy Blocker2Cleared 510(K)
- K201734AllerBlock Junior2Cleared 510(K)
- K170848Alzair Allergy Blocker2Cleared 510(K)
- K134003RHINIX NASAL FILTER2Cleared 510(K)
- K132520NASAL EASE ALLERGY BLOCKER2Cleared 510(K)
- K120894HAYMAX2Cleared 510(K)
- K053625NASALGUARD2Cleared 510(K)
- K042610DR. THEISS ALERGOL POLLEN BLOCKER CREAM2Cleared 510(K)
- Subpart F—Therapeutic DevicesCFR Sub-Part
- Subpart G—General Hospital and Personal Use Miscellaneous DevicesCFR Sub-Part
- Subpart G—Miscellaneous DevicesCFR Sub-Part
- Gastroenterology and UrologyReview Panel
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- Obstetrical and GynecologicalReview Panel
- OphthalmicReview Panel
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- UnknownReview Panel
HAYMAX
- Page Type
- Cleared 510(K)
- PDF* The FDA doesn't provide PDFs for all submissions.
- Analyzed PDF
- 510(k) Number
- K120894
- 510(k) Type
- Traditional
- Applicant
- Haymax Limited
- Country
- United Kingdom
- FDA Decision
- Substantially Equivalent
- Decision Date
- 5/17/2012
- Days to Decision
- 55 days
- Submission Type
- Summary