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FDA 510(k)

INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION

K-Number: K880208 · 1988-04-12

ApplicantDresser Argus, Inc.
Decision Date1988-04-12
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION is the device name listed in this FDA 510(k) record. The listed applicant is Dresser Argus, Inc.. It received FDA 510(k) clearance on 1988-04-12 under 510(k) number K880208. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION?

INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is Dresser Argus, Inc.. The 510(k) number is K880208.

When did INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION receive FDA 510(k) clearance?

INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION received FDA 510(k) clearance on 1988-04-12, under 510(k) number K880208.

Who is the listed applicant for INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION?

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

What is the FDA product code for INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION?

The FDA product code for INVESTIGATION KIT, SEXUAL ASSAULT DETERMINATION is EFQ.

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.

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Other records listing Dresser Argus, 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.

K905304DRESSER ARGUS P/N 1818

Related Devices (Code: EFQ)

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.

K991757NON-ABSORBABLE GAUZE FOR EXTERNAL USE, STERILE AND NON STERILEFurlong IndustriesK991215SYMTEX GAUZE PADS (1'S) AND SYMTEX GAUZE SPONGES STERILE 2'S AND STERILE 10'SSymtex Healthcare Corp.K990974VITOP DRESSINGWonder & Bioenergy Hi-Tech America, Inc.K990584GAUZE SPONGES: LAPAROTOMY SPONGE, X-RAY DETECTABLEBroadline Medical IndustriesK984187CROSSTEX NON-WOVEN SPONGESCrosstex Intl.K983016GAUZE, SPONGES, CAT # 11-003Vitalcare Group, 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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