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FDA 510(k)

NON-ADHERA ADHESIVE PAD 3X4

K-Number: K853334 · 1985-08-21

ApplicantAmerican White Cross, Inc.
Decision Date1985-08-21
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NON-ADHERA ADHESIVE PAD 3X4 is the device name listed in this FDA 510(k) record. The listed applicant is American White Cross, Inc.. It received FDA 510(k) clearance on 1985-08-21 under 510(k) number K853334. The device is classified under product code NAD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NON-ADHERA ADHESIVE PAD 3X4?

NON-ADHERA ADHESIVE PAD 3X4 is a medical device that received FDA 510(k) clearance on 1985-08-21. The listed applicant is American White Cross, Inc.. The 510(k) number is K853334.

When did NON-ADHERA ADHESIVE PAD 3X4 receive FDA 510(k) clearance?

NON-ADHERA ADHESIVE PAD 3X4 received FDA 510(k) clearance on 1985-08-21, under 510(k) number K853334.

Who is the listed applicant for NON-ADHERA ADHESIVE PAD 3X4?

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

What is the FDA product code for NON-ADHERA ADHESIVE PAD 3X4?

The FDA product code for NON-ADHERA ADHESIVE PAD 3X4 is NAD.

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Other records listing American White Cross, Inc. as applicant

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K964614ULTRAFERA WOUND DRESSINGK962400AIR MAX EXTERNAL NASAL DILATOR STRIPK894802AWC BUTTERFLY WOUND CLOSURESK854809WHITE CROSS STERILE PAD 4IN. X 4IN.K853558DOSIMETRIC RELEASE/RADIATION STERILIZ. ABSORB GAUZK852412NON-ADHERENT PAD

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Related Devices (Code: NAD)

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K254246LT Antibacterial Foam with Silver DressingZhejiang Longterm Medical Technology Co., Ltd.K102403SAM CHEST SEAL WITH VAVLE; SAM CHEST SEALSam Medical ProductsK091133APLION TOPICAL CARE SYSTEMAplion Medical,LlcK072560ENVELA (HYDROHESIVE OCCLUSIVE DRESSING)Teikoku Pharma USA, Inc.K080524CENTURION SORBAVIEW OTCTri-State Hospital Supply Corp.K060046DERMASTREAMEnzysurge , Ltd.

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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