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FDA 510(k)

ZAP-GUARD

K-Number: K896985 · 1990-07-31

ApplicantGuardian Angel Products, Inc.
Decision Date1990-07-31
Product CodeDRL
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZAP-GUARD is the device name listed in this FDA 510(k) record. The listed applicant is Guardian Angel Products, Inc.. It received FDA 510(k) clearance on 1990-07-31 under 510(k) number K896985. The device is classified under product code DRL. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZAP-GUARD?

ZAP-GUARD is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Guardian Angel Products, Inc.. The 510(k) number is K896985.

When did ZAP-GUARD receive FDA 510(k) clearance?

ZAP-GUARD received FDA 510(k) clearance on 1990-07-31, under 510(k) number K896985.

Who is the listed applicant for ZAP-GUARD?

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

What is the FDA product code for ZAP-GUARD?

The FDA product code for ZAP-GUARD is DRL.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Guardian Angel 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.

K030547MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBEK923840NEEDLE-GRABBERK923835THE ELEVENTH FINGERK910687GUARDIAN GEL, SURGEON'S GLOVING CREAM

Related Devices (Code: DRL)

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.

K190437Delta 3300Netech CorporationK182905UniPulseSeaward GroupK110192DEFIBRILLATOR ANALYZER - DA-2006PBc Group International, Inc.K083347IMPULSE 7010 DEFIBRILLATOR SELECTABLE LOADSFluke BiomedicalK072114IMPULSE 6000D/7000DPFluke BiomedicalK062099PHASE 3, MODEL DT-1Datrend Systems, Inc.

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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