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FDA 510(k)

HAWKINS MINI-E.B.A.

K-Number: K862031 · 1986-07-14

ApplicantPb Sales C/O Geller & Bozeman
Decision Date1986-07-14
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

HAWKINS MINI-E.B.A. is the device name listed in this FDA 510(k) record. The listed applicant is Pb Sales C/O Geller & Bozeman. It received FDA 510(k) clearance on 1986-07-14 under 510(k) number K862031. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HAWKINS MINI-E.B.A.?

HAWKINS MINI-E.B.A. is a medical device that received FDA 510(k) clearance on 1986-07-14. The listed applicant is Pb Sales C/O Geller & Bozeman. The 510(k) number is K862031.

When did HAWKINS MINI-E.B.A. receive FDA 510(k) clearance?

HAWKINS MINI-E.B.A. received FDA 510(k) clearance on 1986-07-14, under 510(k) number K862031.

Who is the listed applicant for HAWKINS MINI-E.B.A.?

The FDA 510(k) record lists Pb Sales C/O Geller & Bozeman as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HAWKINS MINI-E.B.A.?

The FDA product code for HAWKINS MINI-E.B.A. is IPF.

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.

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Other records listing Pb Sales C/O Geller & Bozeman 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.

K820761PALM BEACH SEATING SYSTEM

Related Devices (Code: IPF)

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.

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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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