FDA 510(k)

BA-93

K-Number: K811407 · 1981-06-16

Decision Date1981-06-16

Product CodeEJH

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

BA-93 is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1981-06-16 under 510(k) number K811407. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BA-93?

BA-93 is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K811407.

When did BA-93 receive FDA 510(k) clearance?

BA-93 received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811407.

Who is the listed applicant for BA-93?

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

What is the FDA product code for BA-93?

The FDA product code for BA-93 is EJH.

Other records listing Deringer-Ney, 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.

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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.