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)

OPTI-MOL FILTERED PUNCTURE PIN

K-Number: K920306 · 1992-04-06

Decision Date1992-04-06
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OPTI-MOL FILTERED PUNCTURE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Automatic Liquid Packaging, Inc.. It received FDA 510(k) clearance on 1992-04-06 under 510(k) number K920306. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTI-MOL FILTERED PUNCTURE PIN?

OPTI-MOL FILTERED PUNCTURE PIN is a medical device that received FDA 510(k) clearance on 1992-04-06. The listed applicant is Automatic Liquid Packaging, Inc.. The 510(k) number is K920306.

When did OPTI-MOL FILTERED PUNCTURE PIN receive FDA 510(k) clearance?

OPTI-MOL FILTERED PUNCTURE PIN received FDA 510(k) clearance on 1992-04-06, under 510(k) number K920306.

Who is the listed applicant for OPTI-MOL FILTERED PUNCTURE PIN?

The FDA 510(k) record lists Automatic Liquid Packaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OPTI-MOL FILTERED PUNCTURE PIN?

The FDA product code for OPTI-MOL FILTERED PUNCTURE PIN is BTT.

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 Automatic Liquid Packaging, 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.

View all 21 devices →

Related Devices (Code: BTT)

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.

↑