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)

GAUZE PACKING, X-RAY DETECTABLE

K-Number: K882707 · 1988-08-03

ApplicantBioseal
Decision Date1988-08-03
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

GAUZE PACKING, X-RAY DETECTABLE is the device name listed in this FDA 510(k) record. The listed applicant is Bioseal. It received FDA 510(k) clearance on 1988-08-03 under 510(k) number K882707. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAUZE PACKING, X-RAY DETECTABLE?

GAUZE PACKING, X-RAY DETECTABLE is a medical device that received FDA 510(k) clearance on 1988-08-03. The listed applicant is Bioseal. The 510(k) number is K882707.

When did GAUZE PACKING, X-RAY DETECTABLE receive FDA 510(k) clearance?

GAUZE PACKING, X-RAY DETECTABLE received FDA 510(k) clearance on 1988-08-03, under 510(k) number K882707.

Who is the listed applicant for GAUZE PACKING, X-RAY DETECTABLE?

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

What is the FDA product code for GAUZE PACKING, X-RAY DETECTABLE?

The FDA product code for GAUZE PACKING, X-RAY DETECTABLE is GDY.

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 Bioseal 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.

View all 10 devices →

Related Devices (Code: GDY)

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.

↑