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FDA 510(k)

FECAL OCCULT SLIDE TEST KIT

K-Number: K830223 · 1983-03-07

Decision Date1983-03-07
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FECAL OCCULT SLIDE TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Chemical Products, Inc.. It received FDA 510(k) clearance on 1983-03-07 under 510(k) number K830223. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FECAL OCCULT SLIDE TEST KIT?

FECAL OCCULT SLIDE TEST KIT is a medical device that received FDA 510(k) clearance on 1983-03-07. The listed applicant is Cambridge Chemical Products, Inc.. The 510(k) number is K830223.

When did FECAL OCCULT SLIDE TEST KIT receive FDA 510(k) clearance?

FECAL OCCULT SLIDE TEST KIT received FDA 510(k) clearance on 1983-03-07, under 510(k) number K830223.

Who is the listed applicant for FECAL OCCULT SLIDE TEST KIT?

The FDA 510(k) record lists Cambridge Chemical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FECAL OCCULT SLIDE TEST KIT?

The FDA product code for FECAL OCCULT SLIDE TEST KIT is KHE.

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 Cambridge Chemical Products, 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: KHE)

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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