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)

APL BIGGY AGAR(NICKERSON)

K-Number: K853226 · 1985-08-19

Decision Date1985-08-19
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

APL BIGGY AGAR(NICKERSON) is the device name listed in this FDA 510(k) record. The listed applicant is Apl Medical Supplies. It received FDA 510(k) clearance on 1985-08-19 under 510(k) number K853226. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APL BIGGY AGAR(NICKERSON)?

APL BIGGY AGAR(NICKERSON) is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Apl Medical Supplies. The 510(k) number is K853226.

When did APL BIGGY AGAR(NICKERSON) receive FDA 510(k) clearance?

APL BIGGY AGAR(NICKERSON) received FDA 510(k) clearance on 1985-08-19, under 510(k) number K853226.

Who is the listed applicant for APL BIGGY AGAR(NICKERSON)?

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

What is the FDA product code for APL BIGGY AGAR(NICKERSON)?

The FDA product code for APL BIGGY AGAR(NICKERSON) is JSI.

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 Apl Medical Supplies 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 25 devices →

Related Devices (Code: JSI)

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.

↑