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)

DISPO FIBRIN PIPET TIPS B4182-2

K-Number: K820532 · 1982-04-08

Decision Date1982-04-08
Product CodeGIE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DISPO FIBRIN PIPET TIPS B4182-2 is the device name listed in this FDA 510(k) record. The listed applicant is American Scientific Products. It received FDA 510(k) clearance on 1982-04-08 under 510(k) number K820532. The device is classified under product code GIE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPO FIBRIN PIPET TIPS B4182-2?

DISPO FIBRIN PIPET TIPS B4182-2 is a medical device that received FDA 510(k) clearance on 1982-04-08. The listed applicant is American Scientific Products. The 510(k) number is K820532.

When did DISPO FIBRIN PIPET TIPS B4182-2 receive FDA 510(k) clearance?

DISPO FIBRIN PIPET TIPS B4182-2 received FDA 510(k) clearance on 1982-04-08, under 510(k) number K820532.

Who is the listed applicant for DISPO FIBRIN PIPET TIPS B4182-2?

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

What is the FDA product code for DISPO FIBRIN PIPET TIPS B4182-2?

The FDA product code for DISPO FIBRIN PIPET TIPS B4182-2 is GIE.

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 American Scientific 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.

View all 28 devices →

Related Devices (Code: GIE)

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.

↑