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FDA 510(k)

WEIL ONCOMETER (IL 186)

K-Number: K760975 · 1977-01-12

Decision Date1977-01-12
Product CodeJJK
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

WEIL ONCOMETER (IL 186) is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K760975. The device is classified under product code JJK. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEIL ONCOMETER (IL 186)?

WEIL ONCOMETER (IL 186) is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760975.

When did WEIL ONCOMETER (IL 186) receive FDA 510(k) clearance?

WEIL ONCOMETER (IL 186) received FDA 510(k) clearance on 1977-01-12, under 510(k) number K760975.

Who is the listed applicant for WEIL ONCOMETER (IL 186)?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WEIL ONCOMETER (IL 186)?

The FDA product code for WEIL ONCOMETER (IL 186) is JJK.

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 Instrumentation Laboratory CO 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 315 devices →

Related Devices (Code: JJK)

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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