PRESERV PVA FIXATIVE 15ML-FORMALIN PK
K-Number: K834412 · 1984-01-13
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Device Summary
Frequently Asked Questions
What is the PRESERV PVA FIXATIVE 15ML-FORMALIN PK?
PRESERV PVA FIXATIVE 15ML-FORMALIN PK is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Preventive Diagnostics Corp.. The 510(k) number is K834412.
When did PRESERV PVA FIXATIVE 15ML-FORMALIN PK receive FDA 510(k) clearance?
PRESERV PVA FIXATIVE 15ML-FORMALIN PK received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834412.
Who is the listed applicant for PRESERV PVA FIXATIVE 15ML-FORMALIN PK?
The FDA 510(k) record lists Preventive Diagnostics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRESERV PVA FIXATIVE 15ML-FORMALIN PK?
The FDA product code for PRESERV PVA FIXATIVE 15ML-FORMALIN PK is KDT.
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.
Other records listing Preventive Diagnostics 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: KDT)
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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