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FDA 510(k)

SPECIMEN ADAPTOR

K-Number: K822557 · 1982-10-18

ApplicantBemis Health Care
Decision Date1982-10-18
Product CodeBYZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPECIMEN ADAPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Bemis Health Care. It received FDA 510(k) clearance on 1982-10-18 under 510(k) number K822557. The device is classified under product code BYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIMEN ADAPTOR?

SPECIMEN ADAPTOR is a medical device that received FDA 510(k) clearance on 1982-10-18. The listed applicant is Bemis Health Care. The 510(k) number is K822557.

When did SPECIMEN ADAPTOR receive FDA 510(k) clearance?

SPECIMEN ADAPTOR received FDA 510(k) clearance on 1982-10-18, under 510(k) number K822557.

Who is the listed applicant for SPECIMEN ADAPTOR?

The FDA 510(k) record lists Bemis Health Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPECIMEN ADAPTOR?

The FDA product code for SPECIMEN ADAPTOR is BYZ.

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 Bemis Health Care 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.

K885019BEMIS STERILE-CASE FOR USE W/ETHYLENE OXIDE STERI.K822556CRITICAL MEASUREMENT UNITK803206SUCTION PROBEK771737SUCTION CANISTERK7717338 EMESIS BASINK771738MALE URINAL

View all 12 devices →

Related Devices (Code: BYZ)

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.

K925412ELECTROMEDICS TISSUE TRAP/ #TT280Electromedics, Inc.K913643MUCOUS SPECIMEN TRAPMedical Device Inspection Co., Inc.K902883TISSUE/POLYP TRAP SYSTEMTriton Technology, Inc.K841409BUSH NECK W/PLUGWarne Surgical Products, Ltd.K840253ONE-WAY AIR VALVEDelta Medical IndustriesK834467SPECIMEN TRAPMicrovasive

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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