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FDA 510(k)

WEIGHT BAG

K-Number: K941592 · 1994-06-06

ApplicantBiocor, Inc.
Decision Date1994-06-06
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

WEIGHT BAG is the device name listed in this FDA 510(k) record. The listed applicant is Biocor, Inc.. It received FDA 510(k) clearance on 1994-06-06 under 510(k) number K941592. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WEIGHT BAG?

WEIGHT BAG is a medical device that received FDA 510(k) clearance on 1994-06-06. The listed applicant is Biocor, Inc.. The 510(k) number is K941592.

When did WEIGHT BAG receive FDA 510(k) clearance?

WEIGHT BAG received FDA 510(k) clearance on 1994-06-06, under 510(k) number K941592.

Who is the listed applicant for WEIGHT BAG?

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

What is the FDA product code for WEIGHT BAG?

The FDA product code for WEIGHT BAG is KPR.

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 Biocor, 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.

K912861FLU ADMIN/WASTE DISP SYS/PROTEC STA/ADMIN/FLUSH-N-

Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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.

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