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FDA 510(k)

BEAM TECH WOUND DRESSING*

K-Number: K890603 · 1989-05-23

ApplicantBeam Tech , Ltd.
Decision Date1989-05-23
Product CodeNAD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEAM TECH WOUND DRESSING* is the device name listed in this FDA 510(k) record. The listed applicant is Beam Tech , Ltd.. It received FDA 510(k) clearance on 1989-05-23 under 510(k) number K890603. 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 BEAM TECH WOUND DRESSING*?

BEAM TECH WOUND DRESSING* is a medical device that received FDA 510(k) clearance on 1989-05-23. The listed applicant is Beam Tech , Ltd.. The 510(k) number is K890603.

When did BEAM TECH WOUND DRESSING* receive FDA 510(k) clearance?

BEAM TECH WOUND DRESSING* received FDA 510(k) clearance on 1989-05-23, under 510(k) number K890603.

Who is the listed applicant for BEAM TECH WOUND DRESSING*?

The FDA 510(k) record lists Beam Tech , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEAM TECH WOUND DRESSING*?

The FDA product code for BEAM TECH WOUND DRESSING* is NAD.

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Related Devices (Code: NAD)

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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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