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)

CAMCO QUIK STAIN II

K-Number: K781347 · 1978-08-21

Decision Date1978-08-21
Product CodeIAF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CAMCO QUIK STAIN II 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 1978-08-21 under 510(k) number K781347. The device is classified under product code IAF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMCO QUIK STAIN II?

CAMCO QUIK STAIN II is a medical device that received FDA 510(k) clearance on 1978-08-21. The listed applicant is Cambridge Chemical Products, Inc.. The 510(k) number is K781347.

When did CAMCO QUIK STAIN II receive FDA 510(k) clearance?

CAMCO QUIK STAIN II received FDA 510(k) clearance on 1978-08-21, under 510(k) number K781347.

Who is the listed applicant for CAMCO QUIK STAIN II?

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 CAMCO QUIK STAIN II?

The FDA product code for CAMCO QUIK STAIN II is IAF.

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: IAF)

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.

↑