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FDA 510(k)

STERILE DISPOSABLE DRAPE(S)

K-Number: K910468 · 1991-03-21

ApplicantE.M. Adams
Decision Date1991-03-21
Product CodeFZI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERILE DISPOSABLE DRAPE(S) 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 1991-03-21 under 510(k) number K910468. The device is classified under product code FZI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE DISPOSABLE DRAPE(S)?

STERILE DISPOSABLE DRAPE(S) is a medical device that received FDA 510(k) clearance on 1991-03-21. The listed applicant is E.M. Adams. The 510(k) number is K910468.

When did STERILE DISPOSABLE DRAPE(S) receive FDA 510(k) clearance?

STERILE DISPOSABLE DRAPE(S) received FDA 510(k) clearance on 1991-03-21, under 510(k) number K910468.

Who is the listed applicant for STERILE DISPOSABLE DRAPE(S)?

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

What is the FDA product code for STERILE DISPOSABLE DRAPE(S)?

The FDA product code for STERILE DISPOSABLE DRAPE(S) is FZI.

Related Clinical Trials

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Other records listing E.M. Adams 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.

K905173SPLASH GUARDK873978DISPOSABLE BIPOLAR FORCEPSK850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACKK843782DRY TRAY

View all 21 devices →

Related Devices (Code: FZI)

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.

K911132MULTIPLE, SURGICAL DRAPE PACKCentral Georgia Ancillary Health SystemsK854159ELLIPTI-PUNCHAlcon LaboratoriesK772395DAVIS RHYTIDECTOMYEdward Weck, Inc.K772394KALRN FACE-LIFE SCISSORSEdward Weck, Inc.

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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