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FDA 510(k)

STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100

K-Number: K001082 · 2000-06-15

Decision Date2000-06-15
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100 is the device name listed in this FDA 510(k) record. The listed applicant is Stackhouse, Inc.. It received FDA 510(k) clearance on 2000-06-15 under 510(k) number K001082. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100?

STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100 is a medical device that received FDA 510(k) clearance on 2000-06-15. The listed applicant is Stackhouse, Inc.. The 510(k) number is K001082.

When did STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100 receive FDA 510(k) clearance?

STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100 received FDA 510(k) clearance on 2000-06-15, under 510(k) number K001082.

Who is the listed applicant for STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100?

The FDA 510(k) record lists Stackhouse, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100?

The FDA product code for STACKHOUSE SMOKE EVACUATOR, MODELS ST-3000, ST 3100 is FYD.

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 Stackhouse, Inc. 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.

Related Devices (Code: FYD)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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