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FDA 510(k)

SHERWOOD WATER TRAP

K-Number: K812569 · 1981-09-25

ApplicantSherwood Medical Co.
Decision Date1981-09-25
Product CodeBYH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SHERWOOD WATER TRAP 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 1981-09-25 under 510(k) number K812569. The device is classified under product code BYH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHERWOOD WATER TRAP?

SHERWOOD WATER TRAP is a medical device that received FDA 510(k) clearance on 1981-09-25. The listed applicant is Sherwood Medical Co.. The 510(k) number is K812569.

When did SHERWOOD WATER TRAP receive FDA 510(k) clearance?

SHERWOOD WATER TRAP received FDA 510(k) clearance on 1981-09-25, under 510(k) number K812569.

Who is the listed applicant for SHERWOOD WATER TRAP?

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 WATER TRAP?

The FDA product code for SHERWOOD WATER TRAP is BYH.

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Other records listing Sherwood Medical Co. as applicant

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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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