FDA 510(k)

INSTRUMENT POCKET

K-Number: K850063 · 1985-02-21

Decision Date1985-02-21

Product Code

DecisionSubstantially Equivalent

Device Summary

INSTRUMENT POCKET is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1985-02-21 under 510(k) number K850063. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT POCKET?

INSTRUMENT POCKET is a medical device that received FDA 510(k) clearance on 1985-02-21. The listed applicant is E.M. Adams. The 510(k) number is K850063.

When did INSTRUMENT POCKET receive FDA 510(k) clearance?

INSTRUMENT POCKET received FDA 510(k) clearance on 1985-02-21, under 510(k) number K850063.

Who is the listed applicant for INSTRUMENT POCKET?

The FDA 510(k) record lists E.M. Adams as the applicant. This does not by itself establish the device manufacturer.

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 E.M. Adams as applicant

K905173SPLASH GUARD K910468STERILE DISPOSABLE DRAPE(S)K873978DISPOSABLE BIPOLAR FORCEPS K843724I.V. START KIT & OBSTETRICAL KIT K843783WET PACK K843782DRY TRAY

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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.