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FDA 510(k)

ZEPPELIN INSTRUMENTS

K-Number: K902850 · 1990-07-18

ApplicantRuggles Corp.
Decision Date1990-07-18
Product CodeHAO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ZEPPELIN INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Ruggles Corp.. It received FDA 510(k) clearance on 1990-07-18 under 510(k) number K902850. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEPPELIN INSTRUMENTS?

ZEPPELIN INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Ruggles Corp.. The 510(k) number is K902850.

When did ZEPPELIN INSTRUMENTS receive FDA 510(k) clearance?

ZEPPELIN INSTRUMENTS received FDA 510(k) clearance on 1990-07-18, under 510(k) number K902850.

Who is the listed applicant for ZEPPELIN INSTRUMENTS?

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

What is the FDA product code for ZEPPELIN INSTRUMENTS?

The FDA product code for ZEPPELIN INSTRUMENTS is HAO.

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Other records listing Ruggles Corp. 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.

K903485TITANIUM MESHK902818MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENTK902819LAMINECTOMY ROGEURK893415TRANS-ORAL DEPTH GAUGE

Related Devices (Code: HAO)

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.

K220920Matreneu Percutaneous Balloon Compression KitShenzhen Shineyard Medical Device Co. , Ltd.K940973MULLAN GANGLION MICROCOMPRESSION SETCook, Inc.K951492RIB RESECTORUnited States Surgical, A Division of Tyco HealthcK943115AUTO SUTURE PITUITARY SPINAL RONGEURUnited States Surgical, A Division of Tyco HealthcK942967AUTO SUTURE SPINAL CURETTEUnited States Surgical, A Division of Tyco HealthcK942969AUTO SUTURE SPINAL NERVE HOOKUnited States Surgical, A Division of Tyco Healthc

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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