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FDA 510(k)

DROPSTIRS - PLASTIC DISPOSABLE PIPET

K-Number: K850800 · 1985-04-02

Decision Date1985-04-02
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DROPSTIRS - PLASTIC DISPOSABLE PIPET is the device name listed in this FDA 510(k) record. The listed applicant is Berwick Medical Products, Inc.. It received FDA 510(k) clearance on 1985-04-02 under 510(k) number K850800. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DROPSTIRS - PLASTIC DISPOSABLE PIPET?

DROPSTIRS - PLASTIC DISPOSABLE PIPET is a medical device that received FDA 510(k) clearance on 1985-04-02. The listed applicant is Berwick Medical Products, Inc.. The 510(k) number is K850800.

When did DROPSTIRS - PLASTIC DISPOSABLE PIPET receive FDA 510(k) clearance?

DROPSTIRS - PLASTIC DISPOSABLE PIPET received FDA 510(k) clearance on 1985-04-02, under 510(k) number K850800.

Who is the listed applicant for DROPSTIRS - PLASTIC DISPOSABLE PIPET?

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

What is the FDA product code for DROPSTIRS - PLASTIC DISPOSABLE PIPET?

The FDA product code for DROPSTIRS - PLASTIC DISPOSABLE PIPET is JQW.

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 Berwick Medical 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: JQW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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