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FDA 510(k)

DISPOSABLE MICROTOME BLADE

K-Number: K831308 · 1983-05-16

Decision Date1983-05-16
Product CodeIDL
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE MICROTOME BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Surgipath Medical Industries, Inc.. It received FDA 510(k) clearance on 1983-05-16 under 510(k) number K831308. The device is classified under product code IDL. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE MICROTOME BLADE?

DISPOSABLE MICROTOME BLADE is a medical device that received FDA 510(k) clearance on 1983-05-16. The listed applicant is Surgipath Medical Industries, Inc.. The 510(k) number is K831308.

When did DISPOSABLE MICROTOME BLADE receive FDA 510(k) clearance?

DISPOSABLE MICROTOME BLADE received FDA 510(k) clearance on 1983-05-16, under 510(k) number K831308.

Who is the listed applicant for DISPOSABLE MICROTOME BLADE?

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 DISPOSABLE MICROTOME BLADE?

The FDA product code for DISPOSABLE MICROTOME BLADE is IDL.

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.

View all 30 devices →

Related Devices (Code: IDL)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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