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FDA 510(k)

FABFOAM #302

K-Number: K894683 · 1989-09-07

ApplicantJewell Industries
Decision Date1989-09-07
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FABFOAM #302 is the device name listed in this FDA 510(k) record. The listed applicant is Jewell Industries. It received FDA 510(k) clearance on 1989-09-07 under 510(k) number K894683. The device is classified under product code JAD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FABFOAM #302?

FABFOAM #302 is a medical device that received FDA 510(k) clearance on 1989-09-07. The listed applicant is Jewell Industries. The 510(k) number is K894683.

When did FABFOAM #302 receive FDA 510(k) clearance?

FABFOAM #302 received FDA 510(k) clearance on 1989-09-07, under 510(k) number K894683.

Who is the listed applicant for FABFOAM #302?

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

What is the FDA product code for FABFOAM #302?

The FDA product code for FABFOAM #302 is JAD.

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Related Devices (Code: JAD)

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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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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