TISSUE CASSETTES FOR PROCESSING-EM BED
K-Number: K831334 · 1983-05-25
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Device Summary
Frequently Asked Questions
What is the TISSUE CASSETTES FOR PROCESSING-EM BED?
TISSUE CASSETTES FOR PROCESSING-EM BED is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K831334.
When did TISSUE CASSETTES FOR PROCESSING-EM BED receive FDA 510(k) clearance?
TISSUE CASSETTES FOR PROCESSING-EM BED received FDA 510(k) clearance on 1983-05-25, under 510(k) number K831334.
Who is the listed applicant for TISSUE CASSETTES FOR PROCESSING-EM BED?
The FDA 510(k) record lists Surgipath Medical Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TISSUE CASSETTES FOR PROCESSING-EM BED?
The FDA product code for TISSUE CASSETTES FOR PROCESSING-EM BED is IDZ.
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 Surgipath Medical Industries, 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: IDZ)
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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