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FDA 510(k)

SAMPLER, FLAMELESS (IL MODEL 555)

K-Number: K760119 · 1976-07-20

Decision Date1976-07-20
Product CodeJXR
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SAMPLER, FLAMELESS (IL MODEL 555) 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 1976-07-20 under 510(k) number K760119. The device is classified under product code JXR. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAMPLER, FLAMELESS (IL MODEL 555)?

SAMPLER, FLAMELESS (IL MODEL 555) is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K760119.

When did SAMPLER, FLAMELESS (IL MODEL 555) receive FDA 510(k) clearance?

SAMPLER, FLAMELESS (IL MODEL 555) received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760119.

Who is the listed applicant for SAMPLER, FLAMELESS (IL MODEL 555)?

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 SAMPLER, FLAMELESS (IL MODEL 555)?

The FDA product code for SAMPLER, FLAMELESS (IL MODEL 555) is JXR.

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: JXR)

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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