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FDA 510(k)

JOAN II

K-Number: K982648 · 1998-09-30

ApplicantCelanese Acetate Co.
Decision Date1998-09-30
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

JOAN II is the device name listed in this FDA 510(k) record. The listed applicant is Celanese Acetate Co.. It received FDA 510(k) clearance on 1998-09-30 under 510(k) number K982648. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOAN II?

JOAN II is a medical device that received FDA 510(k) clearance on 1998-09-30. The listed applicant is Celanese Acetate Co.. The 510(k) number is K982648.

When did JOAN II receive FDA 510(k) clearance?

JOAN II received FDA 510(k) clearance on 1998-09-30, under 510(k) number K982648.

Who is the listed applicant for JOAN II?

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

What is the FDA product code for JOAN II?

The FDA product code for JOAN II is EFQ.

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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