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FDA 510(k)

SHERWOOD VENTILATORY MUSCLE TRAINER

K-Number: K802165 · 1980-09-26

Decision Date1980-09-26
Product CodeBYW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHERWOOD VENTILATORY MUSCLE TRAINER 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 1980-09-26 under 510(k) number K802165. The device is classified under product code BYW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERWOOD VENTILATORY MUSCLE TRAINER?

SHERWOOD VENTILATORY MUSCLE TRAINER is a medical device that received FDA 510(k) clearance on 1980-09-26. The listed applicant is Sherwood Medical Co.. The 510(k) number is K802165.

When did SHERWOOD VENTILATORY MUSCLE TRAINER receive FDA 510(k) clearance?

SHERWOOD VENTILATORY MUSCLE TRAINER received FDA 510(k) clearance on 1980-09-26, under 510(k) number K802165.

Who is the listed applicant for SHERWOOD VENTILATORY MUSCLE TRAINER?

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 SHERWOOD VENTILATORY MUSCLE TRAINER?

The FDA product code for SHERWOOD VENTILATORY MUSCLE TRAINER is BYW.

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 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.

View all 191 devices →

Related Devices (Code: BYW)

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.

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