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FDA 510(k)

METATECH ROBINSON BOLT ACCESSORY

K-Number: K882552 · 1988-09-08

ApplicantMetatech Corp.
Decision Date1988-09-08
Product CodeGWM
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

METATECH ROBINSON BOLT ACCESSORY is the device name listed in this FDA 510(k) record. The listed applicant is Metatech Corp.. It received FDA 510(k) clearance on 1988-09-08 under 510(k) number K882552. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METATECH ROBINSON BOLT ACCESSORY?

METATECH ROBINSON BOLT ACCESSORY is a medical device that received FDA 510(k) clearance on 1988-09-08. The listed applicant is Metatech Corp.. The 510(k) number is K882552.

When did METATECH ROBINSON BOLT ACCESSORY receive FDA 510(k) clearance?

METATECH ROBINSON BOLT ACCESSORY received FDA 510(k) clearance on 1988-09-08, under 510(k) number K882552.

Who is the listed applicant for METATECH ROBINSON BOLT ACCESSORY?

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

What is the FDA product code for METATECH ROBINSON BOLT ACCESSORY?

The FDA product code for METATECH ROBINSON BOLT ACCESSORY is GWM.

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Other records listing Metatech Corp. as applicant

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K924314MOBILE STANDING FRAMEK915370COPPER VAPOR LASER SYSTEMK903883VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LESK890865HEXASCAN SCANNER HANDPIECEK883541METALASER VASCULASEK883881MODIFIED MODEL 2001 FIBER OPTICS CATHETER

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Related Devices (Code: GWM)

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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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