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FDA 510(k)

ARGYLE ROB-NELS

K-Number: K810216 · 1981-02-09

ApplicantSherwood Medical Co.
Decision Date1981-02-09
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ARGYLE ROB-NELS is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1981-02-09 under 510(k) number K810216. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGYLE ROB-NELS?

ARGYLE ROB-NELS is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Sherwood Medical Co.. The 510(k) number is K810216.

When did ARGYLE ROB-NELS receive FDA 510(k) clearance?

ARGYLE ROB-NELS received FDA 510(k) clearance on 1981-02-09, under 510(k) number K810216.

Who is the listed applicant for ARGYLE ROB-NELS?

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

What is the FDA product code for ARGYLE ROB-NELS?

The FDA product code for ARGYLE ROB-NELS is KOD.

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Other records listing Sherwood Medical 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.

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Related Devices (Code: KOD)

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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