POST-MYDS(TM)
K-Number: K930840 · 1994-03-01
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Device Summary
Frequently Asked Questions
What is the POST-MYDS(TM)?
POST-MYDS(TM) is a medical device that received FDA 510(k) clearance on 1994-03-01. The listed applicant is Aukland Medical Plastics, Inc.. The 510(k) number is K930840.
When did POST-MYDS(TM) receive FDA 510(k) clearance?
POST-MYDS(TM) received FDA 510(k) clearance on 1994-03-01, under 510(k) number K930840.
Who is the listed applicant for POST-MYDS(TM)?
The FDA 510(k) record lists Aukland Medical Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POST-MYDS(TM)?
The FDA product code for POST-MYDS(TM) is HOY.
Other records listing Aukland Medical Plastics, 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.
Related Devices (Code: HOY)
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.
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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