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FDA 510(k)

FINGER BONIOMETER BK7506

K-Number: K831550 · 1983-06-24

ApplicantFred Sammons, Inc.
Decision Date1983-06-24
Product CodeKQW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FINGER BONIOMETER BK7506 is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1983-06-24 under 510(k) number K831550. The device is classified under product code KQW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FINGER BONIOMETER BK7506?

FINGER BONIOMETER BK7506 is a medical device that received FDA 510(k) clearance on 1983-06-24. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831550.

When did FINGER BONIOMETER BK7506 receive FDA 510(k) clearance?

FINGER BONIOMETER BK7506 received FDA 510(k) clearance on 1983-06-24, under 510(k) number K831550.

Who is the listed applicant for FINGER BONIOMETER BK7506?

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

What is the FDA product code for FINGER BONIOMETER BK7506?

The FDA product code for FINGER BONIOMETER BK7506 is KQW.

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Other records listing Fred Sammons, 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.

K880644ULTRA-PAN FOR ORTHOTIC PLASTICS (7262)K880647ADULT PERCEPTUAL MOTOR PUZZLES (5331-01)K831549ARM SLINGSK831548SPLINTSK831544DELUXE TRACTION EXERCISE GLOVE BK5035K831542ADJUSTABLE POLYCENTRIC ELBOW HINGE

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Related Devices (Code: KQW)

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.

K926237O'BRIEN GONIOMETERSgarlato Laboratories, Inc.K901744DOBBHOFF(R) RETRIEVAL FORCEPSBiosearch Medical Products, Inc.K870767THE (CROM) TESTERTwin City Surgical, Inc.K850082HAND HELD GONIOMETERChattanooga Group, Inc.K812778THE TELOS EQUIPMENTThe Telos Co.K810441UNIVERSAL GONIMETERFred Sammons, 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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