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FDA 510(k)

INSTRUMENT AND ACCESSORY KIT

K-Number: K780488 · 1978-04-12

Decision Date1978-04-12
Product CodeKDD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT AND ACCESSORY 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 1978-04-12 under 510(k) number K780488. The device is classified under product code KDD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT AND ACCESSORY KIT?

INSTRUMENT AND ACCESSORY KIT is a medical device that received FDA 510(k) clearance on 1978-04-12. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K780488.

When did INSTRUMENT AND ACCESSORY KIT receive FDA 510(k) clearance?

INSTRUMENT AND ACCESSORY KIT received FDA 510(k) clearance on 1978-04-12, under 510(k) number K780488.

Who is the listed applicant for INSTRUMENT AND ACCESSORY 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 INSTRUMENT AND ACCESSORY KIT?

The FDA product code for INSTRUMENT AND ACCESSORY KIT is KDD.

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: KDD)

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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