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FDA 510(k)

HILL TOP CHAMBER

K-Number: K811365 · 1981-08-20

ApplicantHill Top Research, Inc.
Decision Date1981-08-20
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HILL TOP CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Hill Top Research, Inc.. It received FDA 510(k) clearance on 1981-08-20 under 510(k) number K811365. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HILL TOP CHAMBER?

HILL TOP CHAMBER is a medical device that received FDA 510(k) clearance on 1981-08-20. The listed applicant is Hill Top Research, Inc.. The 510(k) number is K811365.

When did HILL TOP CHAMBER receive FDA 510(k) clearance?

HILL TOP CHAMBER received FDA 510(k) clearance on 1981-08-20, under 510(k) number K811365.

Who is the listed applicant for HILL TOP CHAMBER?

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

What is the FDA product code for HILL TOP CHAMBER?

The FDA product code for HILL TOP CHAMBER is KXF.

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Related Devices (Code: KXF)

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

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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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