Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HYDRASORB JOYCE SPONGE

K-Number: K925841 · 1993-05-12

ApplicantAvitar, Inc.
Decision Date1993-05-12
Product CodeNAC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HYDRASORB JOYCE SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Avitar, Inc.. It received FDA 510(k) clearance on 1993-05-12 under 510(k) number K925841. The device is classified under product code NAC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYDRASORB JOYCE SPONGE?

HYDRASORB JOYCE SPONGE is a medical device that received FDA 510(k) clearance on 1993-05-12. The listed applicant is Avitar, Inc.. The 510(k) number is K925841.

When did HYDRASORB JOYCE SPONGE receive FDA 510(k) clearance?

HYDRASORB JOYCE SPONGE received FDA 510(k) clearance on 1993-05-12, under 510(k) number K925841.

Who is the listed applicant for HYDRASORB JOYCE SPONGE?

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

What is the FDA product code for HYDRASORB JOYCE SPONGE?

The FDA product code for HYDRASORB JOYCE SPONGE is NAC.

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.

Other records listing Avitar, 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.

Related Devices (Code: NAC)

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.

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.

↑