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FDA 510(k)

INSTA-HOLD

K-Number: K822847 · 1982-10-08

ApplicantTaub Industries
Decision Date1982-10-08
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTA-HOLD is the device name listed in this FDA 510(k) record. The listed applicant is Taub Industries. It received FDA 510(k) clearance on 1982-10-08 under 510(k) number K822847. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTA-HOLD?

INSTA-HOLD is a medical device that received FDA 510(k) clearance on 1982-10-08. The listed applicant is Taub Industries. The 510(k) number is K822847.

When did INSTA-HOLD receive FDA 510(k) clearance?

INSTA-HOLD received FDA 510(k) clearance on 1982-10-08, under 510(k) number K822847.

Who is the listed applicant for INSTA-HOLD?

The FDA 510(k) record lists Taub Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTA-HOLD?

The FDA product code for INSTA-HOLD is KKX.

Related Clinical Trials

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Other records listing Taub Industries 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.

K880513DISP. NON-MAGNETIC SURGICAL INSTRU. DRAPE

Related Devices (Code: KKX)

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.

K230645BeneHold™ Surgical Incise Drape with CHG antimicrobial IIAvery Dennison Medical , Ltd.K2225783M™ Ioban™ CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)3M CompanyK202208BeneHold Surgical Incise Drape with CHG antimicrobialAvery Dennison Belgie BvbaK200238ControlRad Sterile CoverControlrad, Inc.K163556MediClear PreOpCovalontechnologies, Inc.K130404TIBURON SURGICAL DRAPECardinal Health200, LLC

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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