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)

ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN

K-Number: K851903 · 1985-07-02

Decision Date1985-07-02
Product CodeEJI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN is the device name listed in this FDA 510(k) record. The listed applicant is Astra Pharmaceutical Products, Inc.. It received FDA 510(k) clearance on 1985-07-02 under 510(k) number K851903. The device is classified under product code EJI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN?

ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN is a medical device that received FDA 510(k) clearance on 1985-07-02. The listed applicant is Astra Pharmaceutical Products, Inc.. The 510(k) number is K851903.

When did ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN receive FDA 510(k) clearance?

ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN received FDA 510(k) clearance on 1985-07-02, under 510(k) number K851903.

Who is the listed applicant for ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN?

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

What is the FDA product code for ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN?

The FDA product code for ASTRA LIGHTWEIGHT STAINLESS STEEL SELF ASPIR/SYRIN is EJI.

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 Astra Pharmaceutical Products, 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: EJI)

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.

↑