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FDA 510(k)

ROCKET INTRAUTERINE DEPTH SOUND

K-Number: K884684 · 1988-12-20

ApplicantA & A Medical, Inc.
Decision Date1988-12-20
Product CodeHHM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ROCKET INTRAUTERINE DEPTH SOUND is the device name listed in this FDA 510(k) record. The listed applicant is A & A Medical, Inc.. It received FDA 510(k) clearance on 1988-12-20 under 510(k) number K884684. The device is classified under product code HHM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROCKET INTRAUTERINE DEPTH SOUND?

ROCKET INTRAUTERINE DEPTH SOUND is a medical device that received FDA 510(k) clearance on 1988-12-20. The listed applicant is A & A Medical, Inc.. The 510(k) number is K884684.

When did ROCKET INTRAUTERINE DEPTH SOUND receive FDA 510(k) clearance?

ROCKET INTRAUTERINE DEPTH SOUND received FDA 510(k) clearance on 1988-12-20, under 510(k) number K884684.

Who is the listed applicant for ROCKET INTRAUTERINE DEPTH SOUND?

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

What is the FDA product code for ROCKET INTRAUTERINE DEPTH SOUND?

The FDA product code for ROCKET INTRAUTERINE DEPTH SOUND is HHM.

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Other records listing A & A Medical, 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.

K013491HSG CATHETER SET, 5F MODEL RGS0947, HSG CATHETER SET, 7F, MODEL R65-948K013437SF SH CATHETER, MODEL R65-945K003949TACKER, MODEL R65-933K011512MMODIFICATION TO LAMINARIAK010510BALLOON CANNULA, SHORT, MODEL R65-985; BALLOON CANNULA, LONG, MODEL R65-985-1K010789CANNULA, SURGICAL GENERAL & PLASTIC SURGERY, MODELR65-995, R65-995-1, R65-995-2, R65-997, R65-997-1

View all 23 devices →

Related Devices (Code: HHM)

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.

K011840CERVILENZ UTERINE MEASURING SOUNDCervilenz, Inc.K935665INTRAUTERINE SOUNDRocket of London, Ltd.K883806ROCKET INTRAUTERINE SOUNDA & A Medical, Inc.K870550TEFLON UTERINE SOUNDCook Ob/GynK840380UTERINE SOUNDIntl. Medical Technologies, Inc.K831224AUGROS HYSTEROMETERAxcan Scientific Corp.

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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