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FDA 510(k)

DISPOSABLE TUBING SETS

K-Number: K820680 · 1982-04-09

Decision Date1982-04-09
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE TUBING SETS is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Surgical Products, Inc.. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820680. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE TUBING SETS?

DISPOSABLE TUBING SETS is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Innovative Surgical Products, Inc.. The 510(k) number is K820680.

When did DISPOSABLE TUBING SETS receive FDA 510(k) clearance?

DISPOSABLE TUBING SETS received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820680.

Who is the listed applicant for DISPOSABLE TUBING SETS?

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

What is the FDA product code for DISPOSABLE TUBING SETS?

The FDA product code for DISPOSABLE TUBING SETS is KYG.

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 Innovative Surgical 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 12 devices →

Related Devices (Code: KYG)

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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