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FDA 510(k)

DETECTO MODEL 6700 SERIES

K-Number: K924847 · 1993-05-24

ApplicantCardinal Scale Mfg. Co.
Decision Date1993-05-24
Product CodeFRW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DETECTO MODEL 6700 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Scale Mfg. Co.. It received FDA 510(k) clearance on 1993-05-24 under 510(k) number K924847. The device is classified under product code FRW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DETECTO MODEL 6700 SERIES?

DETECTO MODEL 6700 SERIES is a medical device that received FDA 510(k) clearance on 1993-05-24. The listed applicant is Cardinal Scale Mfg. Co.. The 510(k) number is K924847.

When did DETECTO MODEL 6700 SERIES receive FDA 510(k) clearance?

DETECTO MODEL 6700 SERIES received FDA 510(k) clearance on 1993-05-24, under 510(k) number K924847.

Who is the listed applicant for DETECTO MODEL 6700 SERIES?

The FDA 510(k) record lists Cardinal Scale Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DETECTO MODEL 6700 SERIES?

The FDA product code for DETECTO MODEL 6700 SERIES is FRW.

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Related Devices (Code: FRW)

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.

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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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