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FDA 510(k)

MULTI-UNIT, MULTI-PURPOSE DEVICE

K-Number: K813638 · 1982-05-07

ApplicantThe Scott & Fetzer Co.
Decision Date1982-05-07
Product CodeEFS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MULTI-UNIT, MULTI-PURPOSE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is The Scott & Fetzer Co.. It received FDA 510(k) clearance on 1982-05-07 under 510(k) number K813638. The device is classified under product code EFS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-UNIT, MULTI-PURPOSE DEVICE?

MULTI-UNIT, MULTI-PURPOSE DEVICE is a medical device that received FDA 510(k) clearance on 1982-05-07. The listed applicant is The Scott & Fetzer Co.. The 510(k) number is K813638.

When did MULTI-UNIT, MULTI-PURPOSE DEVICE receive FDA 510(k) clearance?

MULTI-UNIT, MULTI-PURPOSE DEVICE received FDA 510(k) clearance on 1982-05-07, under 510(k) number K813638.

Who is the listed applicant for MULTI-UNIT, MULTI-PURPOSE DEVICE?

The FDA 510(k) record lists The Scott & Fetzer Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTI-UNIT, MULTI-PURPOSE DEVICE?

The FDA product code for MULTI-UNIT, MULTI-PURPOSE DEVICE is EFS.

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Related Devices (Code: EFS)

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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