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FDA 510(k)

CLEANING AND ISOLATION ROOM KIT

K-Number: K760904 · 1976-12-30

Decision Date1976-12-30
Product CodeFYC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CLEANING AND ISOLATION ROOM KIT is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K760904. The device is classified under product code FYC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANING AND ISOLATION ROOM KIT?

CLEANING AND ISOLATION ROOM KIT is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K760904.

When did CLEANING AND ISOLATION ROOM KIT receive FDA 510(k) clearance?

CLEANING AND ISOLATION ROOM KIT received FDA 510(k) clearance on 1976-12-30, under 510(k) number K760904.

Who is the listed applicant for CLEANING AND ISOLATION ROOM KIT?

The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLEANING AND ISOLATION ROOM KIT?

The FDA product code for CLEANING AND ISOLATION ROOM KIT is FYC.

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 American Hospital Supply Corp. 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 56 devices →

Related Devices (Code: FYC)

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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