Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE MICROTOME BLADES

K-Number: K831921 · 1983-07-29

Decision Date1983-07-29
Product CodeIDL
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE MICROTOME BLADES is the device name listed in this FDA 510(k) record. The listed applicant is Polymer Technology Corp.. It received FDA 510(k) clearance on 1983-07-29 under 510(k) number K831921. 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 BLADES?

DISPOSABLE MICROTOME BLADES is a medical device that received FDA 510(k) clearance on 1983-07-29. The listed applicant is Polymer Technology Corp.. The 510(k) number is K831921.

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

DISPOSABLE MICROTOME BLADES received FDA 510(k) clearance on 1983-07-29, under 510(k) number K831921.

Who is the listed applicant for DISPOSABLE MICROTOME BLADES?

The FDA 510(k) record lists Polymer Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE MICROTOME BLADES?

The FDA product code for DISPOSABLE MICROTOME BLADES 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 Polymer Technology 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.

View all 23 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

View on FDA Database →

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

↑