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FDA 510(k)

GRIP, HOSPITAL UTILITY

K-Number: K781800 · 1978-12-07

ApplicantBaka Manufacturing Co., Inc.
Decision Date1978-12-07
Product CodeKMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GRIP, HOSPITAL UTILITY is the device name listed in this FDA 510(k) record. The listed applicant is Baka Manufacturing Co., Inc.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781800. The device is classified under product code KMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIP, HOSPITAL UTILITY?

GRIP, HOSPITAL UTILITY is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Baka Manufacturing Co., Inc.. The 510(k) number is K781800.

When did GRIP, HOSPITAL UTILITY receive FDA 510(k) clearance?

GRIP, HOSPITAL UTILITY received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781800.

Who is the listed applicant for GRIP, HOSPITAL UTILITY?

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

What is the FDA product code for GRIP, HOSPITAL UTILITY?

The FDA product code for GRIP, HOSPITAL UTILITY is KMK.

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 Baka Manufacturing Co., 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.

K780190CATHETER STRAP & RUINARY BAY HOLDER

Related Devices (Code: KMK)

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.

K180994SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8FInterrad Medical, Inc.K981860A P HARNESSParaworks Enterprise, Ltd.K963365MULTI-PURPOSE MEDICAL TUBE HOLDERByrd Medical Devices, Inc.K941098SECURE-SITEOp-Co Medical Products , Ltd.K943147STATLOCK CVVenetec, Inc.K943047IV START KITSSterile Concepts, Inc.

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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