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FDA 510(k)

TAMPER HAMPER

K-Number: K863872 · 1987-02-10

Decision Date1987-02-10
Product CodeLPZ
DecisionSubstantially Equivalent

Device Summary

TAMPER HAMPER is the device name listed in this FDA 510(k) record. The listed applicant is Hydro-Med Products, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K863872. The device is classified under product code LPZ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPER HAMPER?

TAMPER HAMPER is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Hydro-Med Products, Inc.. The 510(k) number is K863872.

When did TAMPER HAMPER receive FDA 510(k) clearance?

TAMPER HAMPER received FDA 510(k) clearance on 1987-02-10, under 510(k) number K863872.

Who is the listed applicant for TAMPER HAMPER?

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

What is the FDA product code for TAMPER HAMPER?

The FDA product code for TAMPER HAMPER is LPZ.

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 Hydro-Med Products, 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.

View all 13 devices →

Related Devices (Code: LPZ)

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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