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FDA 510(k)

MINI-TIP CULTURETTE

K-Number: K803298 · 1981-01-12

Decision Date1981-01-12
Product CodeJTW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MINI-TIP CULTURETTE is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1981-01-12 under 510(k) number K803298. The device is classified under product code JTW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI-TIP CULTURETTE?

MINI-TIP CULTURETTE is a medical device that received FDA 510(k) clearance on 1981-01-12. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K803298.

When did MINI-TIP CULTURETTE receive FDA 510(k) clearance?

MINI-TIP CULTURETTE received FDA 510(k) clearance on 1981-01-12, under 510(k) number K803298.

Who is the listed applicant for MINI-TIP CULTURETTE?

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

What is the FDA product code for MINI-TIP CULTURETTE?

The FDA product code for MINI-TIP CULTURETTE is JTW.

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 Marion Laboratories, 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 38 devices →

Related Devices (Code: JTW)

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.

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