AUTO MASH
K-Number: K854604 · 1985-12-06
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Device Summary
Frequently Asked Questions
What is the AUTO MASH?
AUTO MASH is a medical device that received FDA 510(k) clearance on 1985-12-06. The listed applicant is Dynatech Corp.. The 510(k) number is K854604.
When did AUTO MASH receive FDA 510(k) clearance?
AUTO MASH received FDA 510(k) clearance on 1985-12-06, under 510(k) number K854604.
Who is the listed applicant for AUTO MASH?
The FDA 510(k) record lists Dynatech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTO MASH?
The FDA product code for AUTO MASH is LIB.
Other records listing Dynatech Corp. 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: LIB)
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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