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)

SPONGES, STANFORD STERILE LAP

K-Number: K790050 · 1979-01-17

Decision Date1979-01-17
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SPONGES, STANFORD STERILE LAP is the device name listed in this FDA 510(k) record. The listed applicant is Stanford Professional Products. It received FDA 510(k) clearance on 1979-01-17 under 510(k) number K790050. 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 SPONGES, STANFORD STERILE LAP?

SPONGES, STANFORD STERILE LAP is a medical device that received FDA 510(k) clearance on 1979-01-17. The listed applicant is Stanford Professional Products. The 510(k) number is K790050.

When did SPONGES, STANFORD STERILE LAP receive FDA 510(k) clearance?

SPONGES, STANFORD STERILE LAP received FDA 510(k) clearance on 1979-01-17, under 510(k) number K790050.

Who is the listed applicant for SPONGES, STANFORD STERILE LAP?

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

What is the FDA product code for SPONGES, STANFORD STERILE LAP?

The FDA product code for SPONGES, STANFORD STERILE LAP 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 Stanford Professional Products 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: 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.

↑